Label: ADVANCED HEALING- petrolatum ointment
- NDC Code(s): 49035-875-17, 49035-875-41
- Packager: Equate
- 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 August 23, 2022
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Uses
- Warnings
- When using this product
- Stop use and ask a doctor if
- Do not use on
- Keep out of reach of children.
- Directions
- Inactive ingredients
- Questions?
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SPL UNCLASSIFIED SECTION
- Paraben free **
- Phthalate free
- Quaternium 15 free**
**This product would not normally contain parabens or quaternium 15
Made in the USA with 90% or more US parts factory certified
This product is not manufactured or distributed by Beiersdorf Inc., distributor Aquaphor Healing Ointment
Satisfaction guaranteed- Or we'll replace it or give you your money back.
For Questions or comments or to report an undesired reaction or side effect, please call 1-888-287-1915
Distributed by: Wal-Mart Stores, Inc.,
Bentonville, AR 72716
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INGREDIENTS AND APPEARANCE
ADVANCED HEALING
petrolatum ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49035-875 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PETROLATUM (UNII: 4T6H12BN9U) (PETROLATUM - UNII:4T6H12BN9U) PETROLATUM 340 mg in 100 g Inactive Ingredients Ingredient Name Strength MINERAL OIL (UNII: T5L8T28FGP) CERESIN (UNII: Q1LS2UJO3A) LANOLIN ALCOHOLS (UNII: 884C3FA9HE) PANTHENOL (UNII: WV9CM0O67Z) GLYCERIN (UNII: PDC6A3C0OX) LEVOMENOL (UNII: 24WE03BX2T) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49035-875-41 396 g in 1 JAR; Type 0: Not a Combination Product 03/20/2017 2 NDC:49035-875-17 50 g in 1 TUBE; Type 0: Not a Combination Product 03/20/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part347 08/27/2013 Labeler - Equate (051957769) Registrant - Vi-Jon, LLC (790752542) Establishment Name Address ID/FEI Business Operations Vi-Jon, LLC 790752542 manufacture(49035-875) Establishment Name Address ID/FEI Business Operations Vi-Jon, LLC 088520668 manufacture(49035-875)