Label: EQUATE SCAR TOPICAL- allantoin cream
- NDC Code(s): 49035-838-17
- Packager: Wal-Mart
- 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 19, 2022
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- SPL UNCLASSIFIED SECTION
- Active ingredient
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- Inactive ingredients
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- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 50 g Tube Carton
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INGREDIENTS AND APPEARANCE
EQUATE SCAR TOPICAL
allantoin creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49035-838 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Allantoin (UNII: 344S277G0Z) (Allantoin - UNII:344S277G0Z) Allantoin 0.005 mg in 1 g Inactive Ingredients Ingredient Name Strength CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E) HUMAN TYPE III COLLAGEN (UNII: 5D8UAE62VB) Methylparaben (UNII: A2I8C7HI9T) Onion (UNII: 492225Q21H) Panthenol (UNII: WV9CM0O67Z) Polyethylene Glycol 400 (UNII: B697894SGQ) Water (UNII: 059QF0KO0R) Alcohol (UNII: 3K9958V90M) Hyaluronate Sodium (UNII: YSE9PPT4TH) Sodium Hydroxide (UNII: 55X04QC32I) Sorbic Acid (UNII: X045WJ989B) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49035-838-17 1 in 1 CARTON 10/18/2018 1 50 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 10/18/2018 Labeler - Wal-Mart (051957769) Establishment Name Address ID/FEI Business Operations Natureplex LLC 062808196 MANUFACTURE(49035-838)