salicylic acid
Generic: medicated callus removers extra thick
Labeler: hebDrug Facts
Product Profile
Brand Name
salicylic acid
Generic Name
medicated callus removers extra thick
Labeler
heb
Dosage Form
PATCH
Routes
Active Ingredients
salicylic acid 40 mg/41
Manufacturer
Identifiers & Regulatory
Product NDC
37808-522
Product ID
37808-522_4872b9b4-a32e-51c7-e063-6294a90a3df8
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M030
Marketing Start
2017-12-22
Marketing End
2027-06-30
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
37808522
Hyphenated Format
37808-522
Supplemental Identifiers
RxCUI
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
salicylic acid (source: ndc)
Generic Name
medicated callus removers extra thick (source: ndc)
Application Number
M030 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 40 mg/41
Packaging
- 4 PATCH in 1 PACKAGE (37808-522-04)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "4872b9b4-a32e-51c7-e063-6294a90a3df8", "openfda": {"unii": ["O414PZ4LPZ"], "rxcui": ["240559"], "spl_set_id": ["51acb7ae-0217-4f35-853b-bdbea858482d"], "manufacturer_name": ["HEB"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "4 PATCH in 1 PACKAGE (37808-522-04)", "package_ndc": "37808-522-04", "marketing_end_date": "20270630", "marketing_start_date": "20171222"}], "brand_name": "Salicylic acid", "product_id": "37808-522_4872b9b4-a32e-51c7-e063-6294a90a3df8", "dosage_form": "PATCH", "product_ndc": "37808-522", "generic_name": "Medicated Callus Removers Extra Thick", "labeler_name": "HEB", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Salicylic acid", "active_ingredients": [{"name": "SALICYLIC ACID", "strength": "40 mg/41"}], "application_number": "M030", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_end_date": "20270630", "marketing_start_date": "20171222"}