Label: ZINC OXIDE paste
- NDC Code(s): 69842-468-26
- Packager: CVS Pharmacy
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated August 20, 2025
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- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Uses
- Warnings
- When using this product
- Stop use and ask a doctor if
- Keep out of reach of children.
- Directions
- Other information
- Inactive ingredients
- Claim
- Disclaimer
- ADVERSE REACTION
- principal display panel
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INGREDIENTS AND APPEARANCE
ZINC OXIDE
zinc oxide pasteProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69842-468 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 400 mg in 1 g Inactive Ingredients Ingredient Name Strength PETROLATUM (UNII: 4T6H12BN9U) COD LIVER OIL (UNII: BBL281NWFG) LANOLIN (UNII: 7EV65EAW6H) STARCH, CORN (UNII: O8232NY3SJ) GLYCERIN (UNII: PDC6A3C0OX) SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A) YELLOW WAX (UNII: 2ZA36H0S2V) TOCOPHEROL (UNII: R0ZB2556P8) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69842-468-26 1 in 1 PACKAGE 03/24/2008 1 113 g in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M016 03/24/2008 Labeler - CVS Pharmacy (062312574) Registrant - Consumer Product Partners, LLC (119091520) Establishment Name Address ID/FEI Business Operations Consumer Product Partners, LLC 119091514 manufacture(69842-468)

