sunscreen
Generic: sunscreen
Labeler: old east main co.Drug Facts
Product Profile
Brand Name
sunscreen
Generic Name
sunscreen
Labeler
old east main co.
Dosage Form
LOTION
Routes
Active Ingredients
avobenzone 30 mg/mL, homosalate 120 mg/mL, octisalate 50 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
75712-950
Product ID
75712-950_4c1f5c71-b7c4-a743-e063-6394a90a584b
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M020
Listing Expiration
2027-12-31
Marketing Start
2024-12-05
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
75712950
Hyphenated Format
75712-950
Supplemental Identifiers
UNII
Packaging Origin
Original Packager
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
sunscreen (source: ndc)
Generic Name
sunscreen (source: ndc)
Application Number
M020 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 30 mg/mL
- 120 mg/mL
- 50 mg/mL
Packaging
- 177 mL in 1 TUBE (75712-950-30)
Packages (1)
Ingredients (3)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "4c1f5c71-b7c4-a743-e063-6394a90a584b", "openfda": {"unii": ["G63QQF2NOX", "V06SV4M95S", "4X49Y0596W"], "spl_set_id": ["1673b8b1-08ad-40a5-8180-93333a8edb67"], "manufacturer_name": ["Old East Main Co."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "177 mL in 1 TUBE (75712-950-30)", "package_ndc": "75712-950-30", "marketing_start_date": "20241205"}], "brand_name": "Sunscreen", "product_id": "75712-950_4c1f5c71-b7c4-a743-e063-6394a90a584b", "dosage_form": "LOTION", "product_ndc": "75712-950", "generic_name": "Sunscreen", "labeler_name": "Old East Main Co.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Sunscreen", "active_ingredients": [{"name": "AVOBENZONE", "strength": "30 mg/mL"}, {"name": "HOMOSALATE", "strength": "120 mg/mL"}, {"name": "OCTISALATE", "strength": "50 mg/mL"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20241205", "listing_expiration_date": "20271231"}