Target Advanced Scar Gel
FDA Label NDC 11673-725

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Target Corporation for the product Target Advanced Scar Gel (NDC 11673-725). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding other, active ingredients, purpose, uses, warnings, when using this product, stop use and ask a doctor if, do not use on, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Other

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

Otc - Keep Out Of Reach Of Children

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

  • Store at room temperature 

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 – Carton

Principal Display Panel – Carton  

Target Up & Up   NDC 11673-0725-27

Advance Scar Gel 

Skin Protectant

NET WT. 0.70 oz (20g)

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