Label: MOISTURE BARRIER- moisture barrier ointment ointment
- NDC Code(s): 43749-231-02
- Packager: Unipack LLC
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated February 13, 2024
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- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Uses
- Warnings
- Do not use on
- When using this product
- Stop use and ask a doctor if
- Keep out of reach of children
- Directions
- Inactive ingredients
- Other information
- Label
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INGREDIENTS AND APPEARANCE
MOISTURE BARRIER
moisture barrier ointment ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:43749-231 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PETROLATUM (UNII: 4T6H12BN9U) (PETROLATUM - UNII:4T6H12BN9U) PETROLATUM 98.3 g in 100 g Inactive Ingredients Ingredient Name Strength COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H) BENZETHONIUM CHLORIDE (UNII: PH41D05744) ALOE VERA LEAF (UNII: ZY81Z83H0X) ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) CORN OIL (UNII: 8470G57WFM) VITAMIN A PALMITATE (UNII: 1D1K0N0VVC) CHOLECALCIFEROL (UNII: 1C6V77QF41) Product Characteristics Color white Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:43749-231-02 56 g in 1 TUBE; Type 0: Not a Combination Product 02/03/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M015 02/03/2018 Labeler - Unipack LLC (009248480) Registrant - Unipack LLC (116015769) Establishment Name Address ID/FEI Business Operations Unipack LLC 009248480 manufacture(43749-231)