Label: LANOLIN, PETROLATUM ointment
- NDC Code(s): 11822-0103-4
- Packager: Rite Aid
- Category: HUMAN OTC DRUG LABEL
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 November 14, 2022
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- Active ingredients
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- Warnings
- Do not use on
- When using this product
- Stop use and ask a doctor if
- Keep out of reach of children
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- Inactive ingredients
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SPL UNCLASSIFIED SECTION
*This product is not manufactured or
distributed by Bayer HealthCare LLC,
distributer of A+D Original Ointment
*Typically this product would not include patabens.
DISTRIBUTED BY:
RITE AID, 30 HUNTER LANE,
CAMP HILL, PA 17011
www.riteaid.com
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INGREDIENTS AND APPEARANCE
LANOLIN, PETROLATUM
lanolin, petrolatum ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11822-0103 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LANOLIN (UNII: 7EV65EAW6H) (LANOLIN - UNII:7EV65EAW6H) LANOLIN 155 mg in 1 g PETROLATUM (UNII: 4T6H12BN9U) (PETROLATUM - UNII:4T6H12BN9U) PETROLATUM 534 mg in 1 g Inactive Ingredients Ingredient Name Strength COD LIVER OIL (UNII: BBL281NWFG) LIGHT MINERAL OIL (UNII: N6K5787QVP) MICROCRYSTALLINE WAX (UNII: XOF597Q3KY) PARAFFIN (UNII: I9O0E3H2ZE) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11822-0103-4 1 in 1 CARTON 08/24/2022 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 final part347 08/24/2022 Labeler - Rite Aid (014578892) Registrant - Vi-Jon, LLC (790752542) Establishment Name Address ID/FEI Business Operations Vi-Jon, LLC 790752542 manufacture(11822-0103) Establishment Name Address ID/FEI Business Operations Vi-Jon, LLC 088520668 manufacture(11822-0103)