salicylic acid
Generic: medicated callus removers
Labeler: harris teeter, llcDrug Facts
Product Profile
Brand Name
salicylic acid
Generic Name
medicated callus removers
Labeler
harris teeter, llc
Dosage Form
PATCH
Routes
Active Ingredients
salicylic acid 40 mg/41
Manufacturer
Identifiers & Regulatory
Product NDC
69256-031
Product ID
69256-031_471f9e1a-f60b-5a80-e063-6294a90a7684
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M030
Listing Expiration
2026-12-31
Marketing Start
2012-01-03
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
69256031
Hyphenated Format
69256-031
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 (source: ndc)
Application Number
M030 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 40 mg/41
Packaging
- 4 PATCH in 1 PACKAGE (69256-031-04)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "471f9e1a-f60b-5a80-e063-6294a90a7684", "openfda": {"unii": ["O414PZ4LPZ"], "rxcui": ["240559"], "spl_set_id": ["0e649195-2e3b-48da-99e6-6f2c7fd686f2"], "manufacturer_name": ["Harris Teeter, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "4 PATCH in 1 PACKAGE (69256-031-04)", "package_ndc": "69256-031-04", "marketing_start_date": "20120103"}], "brand_name": "Salicylic Acid", "product_id": "69256-031_471f9e1a-f60b-5a80-e063-6294a90a7684", "dosage_form": "PATCH", "product_ndc": "69256-031", "generic_name": "Medicated Callus Removers", "labeler_name": "Harris Teeter, LLC", "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_start_date": "20120103", "listing_expiration_date": "20261231"}