Label: LANOLIN, PETROLATUM ointment
- NDC Code(s): 69842-488-26
- Packager: CVS Pharmacy
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated August 6, 2024
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- Active ingredients
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- When using this product
- Stop use and ask a doctor if
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- Inactive ingredients
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SPL UNCLASSIFIED SECTION
This product would not normally contain parabens.
*This product is not manufactured or distributed by Bayer HealthCare LLC, distributor of A+D Original Ointment
Distributed by: CVS Pharmacy, Inc.
One CVS Drive, Woonsocket, RI 02895
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This product would not normally contain parabens
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INGREDIENTS AND APPEARANCE
LANOLIN, PETROLATUM
lanolin, petrolatum ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69842-488 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:69842-488-26 1 in 1 CARTON 12/30/2020 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 Drug M016 12/30/2020 Labeler - CVS Pharmacy (062312574) Registrant - Consumer Product Partners, LLC (119091520) Establishment Name Address ID/FEI Business Operations Consumer Product Partners, LLC 119091514 manufacture(69842-488)