Label: TARGET ADVANCED SCAR GEL- advanced scar gel gel
- NDC Code(s): 11673-725-27
- Packager: Target Corporation
- 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 March 17, 2022
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INGREDIENTS AND APPEARANCE
TARGET ADVANCED SCAR GEL
advanced scar gel gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11673-725 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z) ALLANTOIN 5 mg in 1 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) POLOXAMER 407 (UNII: TUF2IVW3M2) ONION (UNII: 492225Q21H) XANTHAN GUM (UNII: TTV12P4NEE) ALCOHOL (UNII: 3K9958V90M) METHYLPARABEN (UNII: A2I8C7HI9T) Sorbic Acid (UNII: X045WJ989B) PANTHENOL (UNII: WV9CM0O67Z) HYALURONATE SODIUM (UNII: YSE9PPT4TH) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11673-725-27 1 in 1 CARTON 08/15/2020 1 20 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 08/15/2020 Labeler - Target Corporation (006961700) Registrant - Sheffield Pharmaceuticals LLC (151177797) Establishment Name Address ID/FEI Business Operations Sheffield Pharmaceuticals LLC 151177797 MANUFACTURE(11673-725)