Walgreens Advanced Scar Gel

Manufacturer
Walgreens Company
Effective date
2024-11-20
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:38:17

Label at a glance#

ProductWalgreens Advanced Scar Gel
Active ingredientALLANTOIN
Label structure10 sections

Indications and uses

Temporarily protects and helps chapped or cracked skin

Dosage and administration

Apply as needed 

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredients 

OTC - ACTIVE INGREDIENT SECTION

Allantion 0.5%

Purpose

OTC - PURPOSE SECTION

Skin Protectant 

Uses

INDICATIONS & USAGE SECTION

Temporarily protects and helps chapped or cracked skin

Warnings

WARNINGS SECTION

For external use only

When using this product 

OTC - WHEN USING SECTION

  • do not get into eyes 

Stop Use and Ask a Doctor if

OTC - STOP USE SECTION

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

Do Not Use on

OTC - DO NOT USE SECTION

  • deep or puncture wounds
  • animal bites
  • serious burns

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

Apply as needed 

Other information

SPL UNCLASSIFIED SECTION

  • Store at room temperature 

Inactive ingredient

INACTIVE INGREDIENT SECTION

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

Principal Display Panel –Tube

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Principal Display Panel – Tube 

Walgreens NDC 0363-2312-07

Advanced Scar Gel 

0.5% Allantoin 

NET WT. 0.70 oz (20g)

Principal Display Panel –TubePrincipal Display Panel –Tube

Principal Display Panel –TubePrincipal Display Panel –Tube

Principal Display Panel –TubePrincipal Display Panel –Tube

Principal Display Panel – Carton

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Principal Display Panel – Carton  

Walgreens NDC 0363-2312-07

Advance Scar Gel 

Skin Protectant

NET WT. 0.70 oz (20g)

Principal Display Panel – CartonPrincipal Display Panel – Carton

Principal Display Panel – CartonPrincipal Display Panel – Carton

Principal Display Panel – CartonPrincipal Display Panel – Carton

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1442087allantoin 0.5 % Topical GelPSN2
1442087allantoin 0.005 MG/MG Topical GelSCD2
1442087allantoin 0.5 % Topical GelSY2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0363-2312-07Walgreens Advanced Scar Gel20 g in 1 TUBEGEL202
0363-2312-07Walgreens Advanced Scar Gel1 in 1 CARTONGEL12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0363-2312WALGREENS ADVANCED SCAR GEL (ADVANCED SCAR GEL) GEL [WALGREENS COMPANY]2Current NDC, Legacy NDC, 2 package rows20241122_2c040475-a124-485c-933e-66b452f5ab46.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0363-23120363-2312-07

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Walgreens Advanced Scar GelADVANCED SCAR GELWalgreens Company2c040475-a124-485c-933e-66b452f5ab462024-11-20WarningsExact identifier
ndc (package): 0363-2312-07
ndc (product): 0363-2312
ndc11 (package): 00363231207
spl id: fbca3a59-215c-4b21-845e-e175e345cf3a
spl set id: 2c040475-a124-485c-933e-66b452f5ab46

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.