Label: VITAMIN A AND D- lanolin, petrolatum ointment
- NDC Code(s): 69396-009-20
- Packager: Trifecta Pharmaceuticals USA LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated January 17, 2023
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- Active Ingredient
- Purpose
- Uses
- Stop use and ask a doctor
- Keep our of reach of children
- Directions
- Inactive Ingredients
- SPL UNCLASSIFIED SECTION
- Warnings
- STORAGE AND HANDLING
- Packaging
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INGREDIENTS AND APPEARANCE
VITAMIN A AND D
lanolin, petrolatum ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69396-009 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PETROLATUM (UNII: 4T6H12BN9U) (PETROLATUM - UNII:4T6H12BN9U) PETROLATUM 53.4 g in 100 g LANOLIN (UNII: 7EV65EAW6H) (LANOLIN - UNII:7EV65EAW6H) LANOLIN 15.5 g in 100 g Inactive Ingredients Ingredient Name Strength MICROCRYSTALLINE WAX (UNII: XOF597Q3KY) PARAFFIN (UNII: I9O0E3H2ZE) COD LIVER OIL (UNII: BBL281NWFG) MINERAL OIL (UNII: T5L8T28FGP) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69396-009-20 1 in 1 BOX 01/03/2017 1 15 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 01/03/2017 Labeler - Trifecta Pharmaceuticals USA LLC (079424163)