TARGET ADVANCED SCAR GEL- advanced scar gel gel 
Target Corporation

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.

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Advanced Scar Gel

Drug Facts

Active ingredients 

Allantion 0.5%

Purpose

Skin Protectant 

Uses

Temporarily protects and helps chapped or cracked skin

Warnings

For external use only

When using this product 

  • do not get into eyes 

Stop Use and Ask a Doctor if

  • condition worsens
  • symptoms last for more than 7 days or clears up and occur again within a few days 

Do Not Use on

  • deep or puncture wounds
  • animal bites
  • serious burns

Keep out of the reach of children. If swallowed get medical help or contact a Poison Control Center immediately.

Directions

Apply as needed 

Other information

Inactive ingredient

Water (Purified), PEG 300, Allium Cepa (Onion) Bulb Extract, Xanthan Gum, Alcohol, Methylparaben, Sorbic Acid, Panthenol, Sodium Hyaluronate, Fragrance

Principal Display Panel –Tube

Principal Display Panel – Tube 

Target Up & Up           NDC 11637-0725-27

Advanced Scar Gel 

0.5% Allantoin 

NET WT. 0.70 oz (20g)

Principal Display Panel –Tube

Principal Display Panel – Carton

Principal Display Panel – Carton  

Target Up & Up   NDC 11673-0725-27

Advance Scar Gel 

Skin Protectant

NET WT. 0.70 oz (20g)

Principal Display Panel – Carton

TARGET ADVANCED SCAR GEL 
advanced scar gel gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11673-725
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z) ALLANTOIN5 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:11673-725-271 in 1 CARTON08/15/2020
120 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34708/15/2020
Labeler - Target Corporation (006961700)
Registrant - Sheffield Pharmaceuticals LLC (151177797)
Establishment
NameAddressID/FEIBusiness Operations
Sheffield Pharmaceuticals LLC151177797MANUFACTURE(11673-725)

Revised: 3/2022
Document Id: 50f4be79-6dda-4b5a-8966-ecf8b83f8094
Set id: 86c215fe-aad4-45d1-bdb7-cde00a115c5c
Version: 2
Effective Time: 20220317
 
Target Corporation