methyl salicylate 25% cream
Generic: methyl salicylate
Labeler: advanced rx of tennessee, llcDrug Facts
Product Profile
Brand Name
methyl salicylate 25% cream
Generic Name
methyl salicylate
Labeler
advanced rx of tennessee, llc
Dosage Form
CREAM
Routes
Active Ingredients
methyl salicylate 250 mg/g
Manufacturer
Identifiers & Regulatory
Product NDC
80425-0544
Product ID
80425-0544_3bdd3021-d16d-12ea-e063-6394a90ab1e0
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M017
Listing Expiration
2026-12-31
Marketing Start
2025-08-08
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
804250544
Hyphenated Format
80425-0544
Supplemental Identifiers
RxCUI
UNII
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
methyl salicylate 25% cream (source: ndc)
Generic Name
methyl salicylate (source: ndc)
Application Number
M017 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 250 mg/g
Packaging
- 120 g in 1 TUBE (80425-0544-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["CUTANEOUS"], "spl_id": "3bdd3021-d16d-12ea-e063-6394a90ab1e0", "openfda": {"unii": ["LAV5U5022Y"], "rxcui": ["238542"], "spl_set_id": ["3bdd3015-349a-0fac-e063-6394a90afe41"], "manufacturer_name": ["Advanced Rx of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "120 g in 1 TUBE (80425-0544-1)", "package_ndc": "80425-0544-1", "marketing_start_date": "20250808"}], "brand_name": "Methyl Salicylate 25% Cream", "product_id": "80425-0544_3bdd3021-d16d-12ea-e063-6394a90ab1e0", "dosage_form": "CREAM", "product_ndc": "80425-0544", "generic_name": "Methyl Salicylate", "labeler_name": "Advanced Rx of Tennessee, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Methyl Salicylate 25% Cream", "active_ingredients": [{"name": "METHYL SALICYLATE", "strength": "250 mg/g"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250808", "listing_expiration_date": "20261231"}