pain relieving
Generic: menthol
Labeler: safetec of america, inc.Drug Facts
Product Profile
Brand Name
pain relieving
Generic Name
menthol
Labeler
safetec of america, inc.
Dosage Form
GEL
Routes
Active Ingredients
menthol 4 g/100g
Manufacturer
Identifiers & Regulatory
Product NDC
61010-4403
Product ID
61010-4403_10aa8eb6-5d50-bea9-e063-6394a90a3623
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M017
Listing Expiration
2026-12-31
Marketing Start
2019-11-01
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
610104403
Hyphenated Format
61010-4403
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
pain relieving (source: ndc)
Generic Name
menthol (source: ndc)
Application Number
M017 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 4 g/100g
Packaging
- 113.4 g in 1 TUBE (61010-4403-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "10aa8eb6-5d50-bea9-e063-6394a90a3623", "openfda": {"unii": ["L7T10EIP3A"], "rxcui": ["415974"], "spl_set_id": ["52ebf64d-095f-467e-bf51-dd8d33b58c7d"], "manufacturer_name": ["Safetec of America, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "113.4 g in 1 TUBE (61010-4403-1)", "package_ndc": "61010-4403-1", "marketing_start_date": "20191101"}], "brand_name": "Pain Relieving", "product_id": "61010-4403_10aa8eb6-5d50-bea9-e063-6394a90a3623", "dosage_form": "GEL", "product_ndc": "61010-4403", "generic_name": "menthol", "labeler_name": "Safetec of America, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Pain Relieving", "active_ingredients": [{"name": "MENTHOL", "strength": "4 g/100g"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20191101", "listing_expiration_date": "20261231"}