Package 69968-0721-3

Brand: neutrogena sun rescue after sun medicated relief

Generic: camphor (synthetic)
NDC Package

Package Facts

Identity

Package NDC 69968-0721-3
Digits Only 6996807213
Product NDC 69968-0721
Product ID 69968-0721_39525447-e7c2-f726-e063-6294a90a0de1
Description

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

Marketing

Marketing Status
Marketed Since 2021-10-01
Brand neutrogena sun rescue after sun medicated relief
Generic camphor (synthetic)
Sample Package No

Linked Drug Pages (1)

Neutrogena Sun Rescue After Sun Medicated Relief ndc-match (0.95)

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"}