Label: BENZOYL PEROXIDE ACNE MEDICATION- benzoyl peroxide gel
- NDC Code(s): 68071-2307-5
- Packager: NuCare Pharmaceuticals,Inc.
- This is a repackaged label.
- Source NDC Code(s): 0536-1055
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated July 17, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
-
SPL UNCLASSIFIED SECTIONDrug Facts
-
Active ingredientBenzoyl peroxide 5% Purpose - Acne treatment
-
Usefor the treatment of acne
-
WarningsFor external use only - Do not use this medication if you have very sensitive skin or if you are sensitive to benzoyl peroxide. When using this product - n keep away from eyes, lips and ...
-
DirectionsCleanse skin thoroughly before applying medication. Cover the entire affected area with a thin layer 1-3 times daily. If bothersome dryness or peeling occurs, reduce application to once a ...
-
Other information Keep tightly closed. Avoid storing at extreme temperatures (below 40° F and above 100° F).
-
Inactive ingredients carbomer, disodium EDTA, laureth-4, sodium hydroxide, titanium dioxide, water
-
Questions or comments? 1-800-645-2158
-
SPL UNCLASSIFIED SECTIONDistributed by: Rugby Laboratories - 31778 Enterprise Drive - Livonia, MI 48150
-
PRINCIPAL DISPLAY PANEL -
-
INGREDIENTS AND APPEARANCEProduct Information