mencylate pain relieving
Generic: menthol, methyl salicylate
Labeler: puretek corporationDrug Facts
Product Profile
Brand Name
mencylate pain relieving
Generic Name
menthol, methyl salicylate
Labeler
puretek corporation
Dosage Form
CREAM
Routes
Active Ingredients
menthol 20 mg/mL, methyl salicylate 100 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
59088-215
Product ID
59088-215_23734cfb-47fb-fb71-e063-6394a90a85de
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M018
Listing Expiration
2026-12-31
Marketing Start
2023-03-24
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
59088215
Hyphenated Format
59088-215
Supplemental Identifiers
RxCUI
UPC
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
mencylate pain relieving (source: ndc)
Generic Name
menthol, methyl salicylate (source: ndc)
Application Number
M018 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/mL
- 100 mg/mL
Packaging
- 59 mL in 1 JAR (59088-215-05)
Packages (1)
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "23734cfb-47fb-fb71-e063-6394a90a85de", "openfda": {"upc": ["0359088215050"], "unii": ["L7T10EIP3A", "LAV5U5022Y"], "rxcui": ["311503"], "spl_set_id": ["f824de86-9492-2e6b-e053-6294a90a6f2a"], "manufacturer_name": ["PureTek Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "59 mL in 1 JAR (59088-215-05)", "package_ndc": "59088-215-05", "marketing_start_date": "20230324"}], "brand_name": "Mencylate Pain Relieving", "product_id": "59088-215_23734cfb-47fb-fb71-e063-6394a90a85de", "dosage_form": "CREAM", "product_ndc": "59088-215", "generic_name": "Menthol, Methyl Salicylate", "labeler_name": "PureTek Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mencylate", "brand_name_suffix": "Pain Relieving", "active_ingredients": [{"name": "MENTHOL", "strength": "20 mg/mL"}, {"name": "METHYL SALICYLATE", "strength": "100 mg/mL"}], "application_number": "M018", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20230324", "listing_expiration_date": "20261231"}