FDA.reportPublic FDA data

Rite Aid Advanced Scar Gel

Manufacturer
Rite Aid
Effective date
2024-11-21
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:38:29

Label at a glance#

ProductRite Aid 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

Rite Aid NDC 11822-8214-7

Advanced Scar Gel 

0.5% Allantoin -Skin Protectant 

NET WT. 0.70 oz (20g)Principal Display Panel –TubePrincipal Display Panel –Tube

Principal Display Panel –TubePrincipal Display Panel –Tube

Principal Display Panel – Carton

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Rite Aid NDC 11822-8214-7

Advance Scar Gel 

0.5% Allantoin - Skin Protectant

NET WT. 0.70 oz (20g)

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
11822-8214-7Rite Aid Advanced Scar Gel1 in 1 CARTONGEL12
11822-8214-7Rite Aid Advanced Scar Gel20 g in 1 TUBEGEL202

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
11822-8214RITE AID ADVANCED SCAR GEL (ADVANCED SCAR GEL) GEL [RITE AID]2Legacy NDC, 2 package rows20241122_beb0e2ef-a6be-4518-a597-35d0f4bd488a.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
11822-821411822-8214-7

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
ALLANTOIN344S277G0ZACTIB
WATER059QF0KO0RIACT
POLOXAMER 407TUF2IVW3M2IACT
ONION492225Q21HIACT
XANTHAN GUMTTV12P4NEEIACT
ALCOHOL3K9958V90MIACT
METHYLPARABENA2I8C7HI9TIACT
Sorbic AcidX045WJ989BIACT
PANTHENOLWV9CM0O67ZIACT
HYALURONATE SODIUMYSE9PPT4THIACT

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
08d7728b-78eb-485e-9b74-e1abe2a0b2cbbeb0e2ef-a6be-4518-a597-35d0f4bd488a2024-11-21WarningsExact identifier
spl id: 08d7728b-78eb-485e-9b74-e1abe2a0b2cb
spl set id: beb0e2ef-a6be-4518-a597-35d0f4bd488a

Reported adverse events (FAERS/openFDA)#

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