Label: QUALITY CHOICE MAXIMUM STRENGTH ZINC OXIDE- zinc oxide ointment
- NDC Code(s): 63868-500-57
- Packager: Chain Drug Marketing Association Inc
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated December 16, 2022
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- Active ingredient
- Uses
- Warnings
- When using this product
- Stop use and ask a doctor if
- If pregnant or breast-feeding
- Keep out of reach of children
- Directions
- Other information
- Inactive ingredients
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
QUALITY CHOICE MAXIMUM STRENGTH ZINC OXIDE
zinc oxide ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63868-500 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION 40 g in 100 g Inactive Ingredients Ingredient Name Strength .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) LAVENDER OIL (UNII: ZBP1YXW0H8) BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) POLYSORBATE 60 (UNII: CAL22UVI4M) LANOLIN (UNII: 7EV65EAW6H) METHYLPARABEN (UNII: A2I8C7HI9T) PETROLATUM (UNII: 4T6H12BN9U) LIGHT MINERAL OIL (UNII: N6K5787QVP) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:63868-500-57 1 in 1 CARTON 11/11/2019 1 57 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 final part347 11/11/2019 Labeler - Chain Drug Marketing Association Inc (011920774)