neutrogena sun rescue after sun medicated relief

Generic: camphor (synthetic)

Labeler: kenvue brands llc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name neutrogena sun rescue after sun medicated relief
Generic Name camphor (synthetic)
Labeler kenvue brands llc
Dosage Form GEL
Routes
TOPICAL
Active Ingredients

camphor (synthetic) 4.5 mg/g

Manufacturer
Kenvue Brands LLC

Identifiers & Regulatory

Product NDC 69968-0721
Product ID 69968-0721_39525447-e7c2-f726-e063-6294a90a0de1
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M017
Listing Expiration 2026-12-31
Marketing Start 2021-10-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 699680721
Hyphenated Format 69968-0721

Supplemental Identifiers

RxCUI
877057
UPC
0086800103585
UNII
5TJD82A1ET

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name neutrogena sun rescue after sun medicated relief (source: ndc)
Generic Name camphor (synthetic) (source: ndc)
Application Number M017 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 4.5 mg/g
source: ndc
Packaging
  • 85 g in 1 TUBE (69968-0721-3)
source: ndc

Packages (1)

69968-0721-3 85 g in 1 TUBE (69968-0721-3)

Ingredients (1)

camphor (synthetic) (4.5 mg/g)

Linked Drug Pages (1)

Neutrogena Sun Rescue After Sun Medicated Relief ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "39525447-e7c2-f726-e063-6294a90a0de1", "openfda": {"upc": ["0086800103585"], "unii": ["5TJD82A1ET"], "rxcui": ["877057"], "spl_set_id": ["c95c5b64-b90f-1143-e053-2a95a90aa03c"], "manufacturer_name": ["Kenvue Brands LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "85 g in 1 TUBE (69968-0721-3)", "package_ndc": "69968-0721-3", "marketing_start_date": "20211001"}], "brand_name": "Neutrogena Sun Rescue After Sun Medicated Relief", "product_id": "69968-0721_39525447-e7c2-f726-e063-6294a90a0de1", "dosage_form": "GEL", "product_ndc": "69968-0721", "generic_name": "CAMPHOR (SYNTHETIC)", "labeler_name": "Kenvue Brands LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Neutrogena Sun Rescue After Sun Medicated Relief", "active_ingredients": [{"name": "CAMPHOR (SYNTHETIC)", "strength": "4.5 mg/g"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20211001", "listing_expiration_date": "20261231"}