el mata callos
Generic: salicylic acid
Labeler: vitamex usa, corpDrug Facts
Product Profile
Brand Name
el mata callos
Generic Name
salicylic acid
Labeler
vitamex usa, corp
Dosage Form
SOLUTION
Routes
Active Ingredients
salicylic acid 170 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
69469-017
Product ID
69469-017_38429f3a-9adb-1e4f-e063-6294a90ac1a4
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M028
Listing Expiration
2026-12-31
Marketing Start
2024-09-05
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
69469017
Hyphenated Format
69469-017
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
el mata callos (source: ndc)
Generic Name
salicylic acid (source: ndc)
Application Number
M028 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 170 mg/mL
Packaging
- 15 mL in 1 BOTTLE, WITH APPLICATOR (69469-017-05)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "38429f3a-9adb-1e4f-e063-6294a90ac1a4", "openfda": {"unii": ["O414PZ4LPZ"], "rxcui": ["312881"], "spl_set_id": ["21c6206e-9183-3e4f-e063-6394a90a33f7"], "manufacturer_name": ["Vitamex USA, Corp"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "15 mL in 1 BOTTLE, WITH APPLICATOR (69469-017-05)", "package_ndc": "69469-017-05", "marketing_start_date": "20240909"}], "brand_name": "El Mata Callos", "product_id": "69469-017_38429f3a-9adb-1e4f-e063-6294a90ac1a4", "dosage_form": "SOLUTION", "product_ndc": "69469-017", "generic_name": "Salicylic Acid", "labeler_name": "Vitamex USA, Corp", "product_type": "HUMAN OTC DRUG", "brand_name_base": "El Mata Callos", "active_ingredients": [{"name": "SALICYLIC ACID", "strength": "170 mg/mL"}], "application_number": "M028", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240905", "listing_expiration_date": "20261231"}