The purpose of the PPPA is to protect children under 5 from poisonings and deaths that can occur when children open containers of hazardous products and access the contents.
The rules that tell you what a child-resistant package is and what products require such packaging are published in the Code of Federal Regulations in Title 16, Part 1700. Because the Commission may add new rules from time to time, we recommend that you check periodically for new or revised rules in the Code of Federal Regulations. Instructions for accessing the regulations on the Commission’s website or obtaining copies appear at the end of this document.
The PPPA allows the Commission to set rules requiring child-resistant packaging for specific types of products customarily used in or around the household if the Commission determines:
- that those products present a risk of serious injury or serious illness to children under 5 who are able to open the packages of the products and drink, eat, or handle the contents, and
- that technology exists or can be developed to produce child-resistant packaging for such products, that the packaging can be used with modern mass production and assembly techniques, and that the packaging will adequately protect the integrity of the product and not interfere with the product’s intended storage or use.
To date, the Commission has issued rules that require child-resistant packaging for the following types of household products:
Chemical and Cosmetic Products
- the following products that contain 10 percent or more by weight of petroleum distillates: furniture polish and kindling and illuminating products, such as lighter fluid and lamp oil,
- paint solvents that contain 10 percent or more by weight of benzene, toluene, xylene, or petroleum distillates;
- products containing 10 percent or more by weight of low viscosity hydrocarbons, such as some baby oils, bath oils, and cleaning solvents;
- dry products such as granules, flakes, or powders that contain 10 percent or more by weight of sodium or potassium hydroxide, and all other products containing 2 percent or more of these chemicals;
- liquid products containing 4 percent or more by weight of methyl alcohol;
- liquid products containing 10 percent or more by weight of turpentine;
- products containing 10 percent or more by weight of sulfuric acid;
- liquid products containing 10 percent or more by weight of ethylene glycol;
- liquid home permanent wave neutralizers that contain more than 600 mg of sodium bromate or more than 50 mg of potassium bromate;
- liquid glue removers containing more than 500 mg of acetonitrile;
- liquid products containing more than 5 percent methacrylic acid on a weight-to-volume basis;
- products containing more than 50 mg of elemental fluoride in a concentration that is more than 0.5 percent on a weight-to-volume basis for liquids and a weight-to-weight basis for solid products. Please note that drugs and dietary supplements that meet these specifications also require child-resistant packaging;
Mouthwash Products containing 3 grams or more of ethanol. Please note that mouthwashes that are drugs and that have 3 grams or more of ethanol also require child-resistant packaging.
Drugs and Dietary Supplements
- the following products for human use that are intended to be taken orally: aspirin; prescription and controlled drugs; products containing more than 1 gram of acetaminophen, products containing 1 gram or more of ibuprofen; products containing more than the equivalent of 66 mg of diphenhydramine base; and products containing more than 0.045 mg of loperamide;
- liquid products containing more than 5 percent methyl salicylate;
- products containing 250 mg or more of elemental iron in a concentration of 0.025 percent or more on a weight-to-volume basis for liquids and 0.05 percent on a weight-to-weight basis for nonliquids;
- products containing more than 5 mg of lidocaine or 0.5 mg of dibucaine; e) products for human use containing 250 mg or more of naproxen, or more than 50 mg of ketoprofen;
- products containing fluoride and mouthwash containing ethanol. (See the description above.);
- products for human use containing more than 14 mg minoxidil;
- any drug that is available over the counter (OTC), in a dosage form intended to be taken orally, and that contains an active ingredient that was previously available only by prescription.
- products containing the equivalent of 0.08 milligrams or more of an imidazoline.
Liquid Nicotine Containers
- The Child Nicotine Poisoning Prevention Act of 2015 (CNPPA), Pub. L. No. 114-116, was enacted on January 28, 2016, requiring any nicotine provided in a liquid nicotine container sold, offered for sale, manufactured for sale, distributed in commerce, or imported into the United States to be in “special packaging,” as defined by the Poison Prevention Packaging Act (PPPA). Beginning on the effective date of July 26, 2016, any liquid nicotine product, including existing inventory, covered by the CNPPA must be in special packaging that meets the standards in 16 C.F.R. § 1700.15, as determined through testing in accordance with the methods described in 16 C.F.R. § 1700.20. In addition, manufacturers, importers, packagers and repackagers of substances regulated under 16 C.F.R. part 1700 must also certify compliance to those requirements in a General Certificate of Conformity (GCC) as required by the Consumer Product Safety Act (CPSA).
- Please see this industry guidance letter for more information about CPSC’s enforcement efforts concerning liquid nicotine packaging and visit CPSC's GCC Guidance Page for more information on how to construct a GCC and certify your product as compliant with applicable consumer product safety requirements. For additional general guidance related to PPPA, see this page.
- Please note, while the CPSC regulates special packaging of liquid nicotine containers, it does not regulate liquid nicotine substances nor other tobacco and tobacco related products as defined in the CPSA. For regulatory information relating to liquid nicotine and other tobacco products please see this helpful guidance page from the Food and Drug Administration's (FDA) Center for Tobacco Products (CTP).
Each of these regulations covers the amount of the product contained in the immediate package of a single retail sale unit. Please refer to the regulation for each specific product to learn more about exemptions and other limitations and requirements. If you have a question about whether a product offered for sale requires child-resistant packaging, the label of the product should contain information about ingredients that will help you.
A child-resistant package is one that is designed or constructed to be significantly difficult for children under 5 to open or obtain a harmful amount of the contents within a reasonable time. In addition, the package must not be difficult for normal adults to use properly.
For a package to be child resistant, a total of 80 percent of the children tested according to the procedure summarized below must not open the package during a full 10 minutes of testing. Please check below for more information about the level of child resistance required during the first 5 minutes of testing.
To make sure that adults are able to use a child-resistant package properly, 90 percent of adults tested have up to 5 minutes, and then another minute in a second test, to open and close the package so that it is child resistant again.
Before starting a test, you should review the test protocol carefully to make sure that you comply with all of the testing requirements. If you choose not to test a package yourself, we recommend that you find a qualified child-testing laboratory in the United States to perform the test. A list of test firms known to CPSC staff is available from the Office of Compliance.
The test uses at least one, and up to four, test panels of 50 children between the ages of 42 and 51 months to test child-resistant packages. Each panel is divided into three groups–30 percent of the children will be of age 42 through 44 months old; 40 percent of the children will be of age 45 through 48 months old; and 30 percent of the children will be of age 49 through 51 months old. Approximately one-half of the children in each group must be boys. The test procedure allows a 10 percent variation in the number of boys and girls in each group.
Each child in the test panel must have no illness, injury, or disability that would interfere with the child’s ability to test the package. No child may test more than two packages. If a child tests two packages, the packages cannot have the same design. This keeps the child from learning how to open the package.
Two children at a time participate in the test in a well-lighted room that is familiar to them and is free from distractions. The tester gives each child an empty child-resistant package and asks the children to try to open it. Each child has 5 minutes to try to do this.
If a child opens the package, he or she is not tested further and that child’s test is counted as a failure of the package to be child resistant. The tester shows any child who does not open the package in the first 5 minutes how to do so and also tells any child who has not tried to use his or her teeth to try to open the package that it is all right to do so. The child then has 5 more minutes to try to open the package. Any child who succeeds in opening the package in the second 5 minutes is also counted as a failure of the package.
For a package to pass, at least 85 percent of the children tested must be unable to open the package before the children receive the demonstration of how the package works and 80 percent after the demonstration. For the first 50-child test panel, if five or fewer children open the package, the package passes. If 15 or more children open the package, the package fails. In either case, no further testing is necessary. If six through 14 children in the first panel open the package, a second test panel of 50 children needs to be tested. Depending upon the results of that test, the package may pass, fail, or require more testing. Please refer to the regulation for more detail. Testing stops after a fourth panel of children, if the test goes that far.
The test uses a panel of 100 senior adults divided into three groups: 25 adults ages 50 to 54 years old; 25 adults ages 55 to 59 years old; and 50 adults ages 60 to 70 years old. Seventy percent of the participants, ages 50 to 59 and 60 to 70, must be females. The test uses senior adults because they are the group most likely to have trouble using child-resistant packaging. Thus, if senior adults are able to open and properly close a package, younger adults should have little difficulty. Each adult tested must have no obvious, overt mental or physical disability.
Yes. Except for prescription drugs, a manufacturer may package one size of a regulated product in regular packaging that is not child resistant. To take advantage of this option, the manufacturer must provide the product in other popular sizes that are child-resistant and must label the regular package with the statement: “This package for households without young children.” or, for small packages: “Package not child resistant.” Please refer to the regulation for more information about the size and location of these statements on the labels of products.
For prescription drugs, the purchaser may request a pharmacist to package a prescription in a regular package, or the physician, dentist, or other person who writes the prescription may specify in the prescription that the drug can be dispensed in regular packaging.
Child-resistant packaging is not intended for children and therefore, child-resistant packaging does not require third party testing under the CPSIA. However, certificates of compliance are required. If any drug or household substance for children or adults is required by a CPSC regulation to be in child-resistant packaging, the importer or the domestic party that packages the product must issue a certificate of conformity with the special packaging requirements of the PPPA. For additional information CPSIA certification requirements, see CPSC's Testing and Certification page.