Home NDC 69968-0721 Neutrogena Sun Rescue After Sun Medicated Relief
Product NDC 69968-0721
11-digit product format 699680721
Labeler code 69968
Product ID 69968-0721_39525447-e7c2-f726-e063-6294a90a0de1
Type HUMAN OTC DRUG
Nonproprietary name CAMPHOR (SYNTHETIC)
Dosage form GEL
Route TOPICAL
Labeler Kenvue Brands LLC
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2021-10-01
Substance CAMPHOR (SYNTHETIC)
Active strength 4.5 mg/g
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Neutrogena Sun Rescue After Sun Medicated Relief
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CAMPHOR (SYNTHETIC) 4.5 mg/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 5TJD82A1ET Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 877057 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table 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
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69968-0721 NEUTROGENA SUN RESCUE AFTER SUN MEDICATED RELIEF (CAMPHOR (SYNTHETIC)) GEL [KENVUE BRANDS LLC] 3 Current NDC, Legacy NDC, 1 package rows 20241115_c95c5b64-b90f-1143-e053-2a95a90aa03c.zip
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 18 of 153 · 3,057 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 69968-0721-3 69968072103 85 g in 1 TUBE (69968-0721-3) 85 g 2021-10-01 0000-00-00 No No Current