Label: ZINC OXIDE 20%- zinc oxide ointment
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Contains inactivated NDC Code(s)
NDC Code(s): 54162-040-16, 54162-040-28, 54162-040-56 - Packager: GERITREX LLC
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated September 5, 2018
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- Drug Facts
- Active Ingredient
- Purpose
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- Other information
- Inactive ingredients
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ZINC OXIDE 20%
zinc oxide ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:54162-040 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION .2 g in 1 g Inactive Ingredients Ingredient Name Strength MINERAL OIL (UNII: T5L8T28FGP) PETROLATUM (UNII: 4T6H12BN9U) Product Characteristics Color white Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:54162-040-28 28 g in 1 TUBE; Type 0: Not a Combination Product 09/17/2018 2 NDC:54162-040-56 56 g in 1 TUBE; Type 0: Not a Combination Product 09/17/2018 3 NDC:54162-040-16 454 g in 1 JAR; Type 0: Not a Combination Product 09/17/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part347 09/17/2018 Labeler - GERITREX LLC (112796248) Establishment Name Address ID/FEI Business Operations GERITREX LLC 112796248 manufacture(54162-040)