salicylic acid
Generic: wart remover medicated discs
Labeler: cvs pharmacyDrug Facts
Product Profile
Brand Name
salicylic acid
Generic Name
wart remover medicated discs
Labeler
cvs pharmacy
Dosage Form
PATCH
Routes
Active Ingredients
salicylic acid 40 mg/181
Manufacturer
Identifiers & Regulatory
Product NDC
59779-136
Product ID
59779-136_47e6a42b-d305-1c47-e063-6294a90ade6c
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M028
Listing Expiration
2027-12-31
Marketing Start
2014-01-01
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
59779136
Hyphenated Format
59779-136
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
wart remover medicated discs (source: ndc)
Application Number
M028 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 40 mg/181
Packaging
- 18 PATCH in 1 BOX (59779-136-18)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "47e6a42b-d305-1c47-e063-6294a90ade6c", "openfda": {"unii": ["O414PZ4LPZ"], "rxcui": ["240559"], "spl_set_id": ["8560ca4c-f5e7-4473-a4ff-e4361366d7e7"], "manufacturer_name": ["CVS Pharmacy"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "18 PATCH in 1 BOX (59779-136-18)", "package_ndc": "59779-136-18", "marketing_start_date": "20140101"}], "brand_name": "Salicylic Acid", "product_id": "59779-136_47e6a42b-d305-1c47-e063-6294a90ade6c", "dosage_form": "PATCH", "product_ndc": "59779-136", "generic_name": "Wart Remover Medicated Discs", "labeler_name": "CVS Pharmacy", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Salicylic Acid", "active_ingredients": [{"name": "SALICYLIC ACID", "strength": "40 mg/181"}], "application_number": "M028", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20140101", "listing_expiration_date": "20271231"}