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
Neutrogena Sun Rescue After Sun Medicated Relief Gel
- Manufacturer
- Kenvue Brands LLC
- Effective date
- 2025-07-07
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 4
- Source
- full-release
- Hydrated at
- 2026-06-01 01:06:50
Label at a glance#
ProductNeutrogena Sun Rescue After Sun Medicated Relief
Active ingredientCAMPHOR (SYNTHETIC)
Label structure11 sections
Storage and handling
Store at 20°C to 25°C (68°F to 77°F)
Contacts and useful links#
Websitewww.neutrogena.com
www.neutrogena.com
www.neutrogena.comLabel contents#
Full prescribing information#
SPL UNCLASSIFIED SECTION
Drug Facts
Active ingredient
Camphor 0.45%
Purpose
External analgesic
Use
temporarily relieves pain and itching associated with sunburn
Warnings
For external use only.
Flammable: Keep away from fire or flame
OTC - WHEN USING SECTION
When using this product avoid contact with eyes
Stop use and ask a doctor if
- condition worsens
- symptoms persist for more than 7 days or clear up and occur again within a few days
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
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
Other information
- Store at 20°C to 25°C (68°F to 77°F)
Inactive ingredients
Water, Alcohol Denat., Triethanolamine, Carbomer, EDTA
Questions?
Call toll-free 800-299-4786 or 215-273-8755 (collect) or visit www.neutrogena.com
SPL UNCLASSIFIED SECTION
Distributed by:
Kenvue Brands LLC
Summit, NJ 07901
PRINCIPAL DISPLAY PANEL - 85 g Tube Label
NEW
Neutrogena®
DERMATOLOGIST RECOMMENDED BRAND
NEUTROGENA®
SUN
RESCUE
AFTER SUN
MEDICATED RELIEF GEL
CAMPHOR EXTERNAL ANALGESIC
pain relief for sunburn
cools, calms and soothes
skin on contact
NET WT 3.0 OZ (85 g)
DailyMed RxNorm Mappings#
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| 777d68c6-a5ab-e06c-d314-677b0b9af0c8 | Product name | 2 | 20240508 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 69968-0721-3 | Neutrogena Sun Rescue After Sun Medicated Relief | 85 g in 1 TUBE | GEL | 85 | 4 |
Products#
Every source-derived product name is available through these pages.
- Neutrogena Sun Rescue After Sun Medicated Relief
- CAMPHOR (SYNTHETIC)
- CARBOXYPOLYMETHYLENE
- EDETIC ACID
- TROLAMINE
- WATER
- ALCOHOL
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 69968-0721 | 69968-0721-3 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| CARBOXYPOLYMETHYLENE | 0A5MM307FC | IACT |
| EDETIC ACID | 9G34HU7RV0 | IACT |
| TROLAMINE | 9O3K93S3TK | IACT |
| WATER | 059QF0KO0R | IACT |
| ALCOHOL | 3K9958V90M | IACT |
| CAMPHOR (SYNTHETIC) | 5TJD82A1ET | ACTIB |
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 |
|---|---|---|---|---|---|---|
| Neutrogena Sun Rescue After Sun Medicated Relief | CAMPHOR (SYNTHETIC) | Kenvue Brands LLC | c95c5b64-b90f-1143-e053-2a95a90aa03c | 2025-07-07 | Warnings | 69968-0721-3 69968-0721 69968072103 39525447-e7c2-f726-e063-6294a90a0de1 c95c5b64-b90f-1143-e053-2a95a90aa03c |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.