Indications and uses
For the temporary relief of pain and itching associated with sunburn, minor burns, minor cuts, scrapes, insect bites, and minor skin irritations.
Walgreens Sunburn Relief Gel
- Manufacturer
- WALGREEN COMPANY
- Effective date
- 2024-10-14
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 2
- Source
- full-release
- Hydrated at
- 2026-06-01 00:25:23
Label at a glance#
ProductWalgreens Sunburn Relief
Active ingredientMENTHOL
Label structure10 sections
Dosage and administration
Adults and children 2 years of age and older: Apply to affected area not more than 3 to 4 times daily Children under 2 years of age : Ask a doctor.
Label contents#
Full prescribing information#
Active Ingredients
Menthol 0.5%
Purpose
External Analgesic
Uses
For the temporary relief of pain and itching associated with sunburn, minor burns, minor cuts, scrapes, insect bites, and minor skin irritations.
Warnings
For External Use Only
When using this product
avoid contact with eyes. If contact occurs, rinse with water to remove.
Stop use and ask a doctor if
- condition worsens
- symptoms persist for more than 7 days
- symptoms clear up and occur again within a few days
Keep out of reach of children
- If swallowed, seek medical help or contact a Poison Control Center immediately.
Directions
- Adults and children 2 years of age and older: Apply to affected area not more than 3 to 4 times daily
- Children under 2 years of age: Ask a doctor.
Inactive Ingredients:
aloe barbadensis leaf juice, isoceteth-20, triethanolamine, carbomer, allantoin, benzophenone-4, tetrasodium EDTA, propylene glycol, methylparaben, propylparaben, diazolidinyl urea, blue 1, water.
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
DailyMed RxNorm Mappings#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 0363-0966-15 | Walgreens Sunburn Relief | 170 g in 1 TUBE | GEL | 170 | 2 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- Walgreens Sunburn Relief
- Menthol
- ALOE VERA LEAF
- ISOCETETH-20
- TROLAMINE
- CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED)
- SULISOBENZONE
- EDETATE SODIUM
- PROPYLENE GLYCOL
- METHYLPARABEN
- PROPYLPARABEN
- DIAZOLIDINYL UREA
- FD&C BLUE NO. 1
- ALLANTOIN
- WATER
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 0363-0966 | 0363-0966-15 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| ALOE VERA LEAF | ZY81Z83H0X | IACT |
| ISOCETETH-20 | O020065R7Z | IACT |
| TROLAMINE | 9O3K93S3TK | IACT |
| CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) | 4Q93RCW27E | IACT |
| SULISOBENZONE | 1W6L629B4K | IACT |
| EDETATE SODIUM | MP1J8420LU | IACT |
| PROPYLENE GLYCOL | 6DC9Q167V3 | IACT |
| METHYLPARABEN | A2I8C7HI9T | IACT |
| PROPYLPARABEN | Z8IX2SC1OH | IACT |
| DIAZOLIDINYL UREA | H5RIZ3MPW4 | IACT |
| FD&C BLUE NO. 1 | H3R47K3TBD | IACT |
| MENTHOL | L7T10EIP3A | ACTIB |
| ALLANTOIN | 344S277G0Z | IACT |
| WATER | 059QF0KO0R | IACT |
Source Document#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Walgreens Sunburn Relief | MENTHOL | WALGREEN COMPANY | c8967fba-6c28-494b-e053-2995a90acbba | 2024-10-14 | Warnings | 0363-0966-15 0363-0966 00363096615 24740d5a-aba3-0bd4-e063-6394a90ab2ca c8967fba-6c28-494b-e053-2995a90acbba |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.