lynx san a foam
Generic: alcohol
Labeler: abc compounding co., inc.Drug Facts
Product Profile
Brand Name
lynx san a foam
Generic Name
alcohol
Labeler
abc compounding co., inc.
Dosage Form
LIQUID
Routes
Active Ingredients
alcohol .7 mL/mL
Manufacturer
Identifiers & Regulatory
Product NDC
62257-007
Product ID
62257-007_43e51604-57ac-4598-e063-6394a90ae2e8
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M004
Listing Expiration
2026-12-31
Marketing Start
2025-01-13
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
62257007
Hyphenated Format
62257-007
Supplemental Identifiers
RxCUI
UPC
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
lynx san a foam (source: ndc)
Generic Name
alcohol (source: ndc)
Application Number
M004 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .7 mL/mL
Packaging
- 1000 mL in 1 CARTRIDGE (62257-007-10)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "43e51604-57ac-4598-e063-6394a90ae2e8", "openfda": {"upc": ["0711808210774"], "unii": ["3K9958V90M"], "rxcui": ["616805"], "spl_set_id": ["2b987ebc-c73b-edbd-e063-6394a90a1d2d"], "manufacturer_name": ["ABC Compounding Co., Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 mL in 1 CARTRIDGE (62257-007-10)", "package_ndc": "62257-007-10", "marketing_start_date": "20250113"}], "brand_name": "Lynx san a foam", "product_id": "62257-007_43e51604-57ac-4598-e063-6394a90ae2e8", "dosage_form": "LIQUID", "product_ndc": "62257-007", "generic_name": "ALCOHOL", "labeler_name": "ABC Compounding Co., Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Lynx san a foam", "active_ingredients": [{"name": "ALCOHOL", "strength": ".7 mL/mL"}], "application_number": "M004", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250113", "listing_expiration_date": "20261231"}