analgesic

Generic: menthol

Labeler: safetec of america, inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name analgesic
Generic Name menthol
Labeler safetec of america, inc.
Dosage Form SPRAY
Routes
TOPICAL
Active Ingredients

menthol 70 mg/L

Manufacturer
Safetec of America, Inc.

Identifiers & Regulatory

Product NDC 61010-8201
Product ID 61010-8201_10981167-c8a2-e068-e063-6394a90ab165
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M017
Listing Expiration 2026-12-31
Marketing Start 2018-09-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 610108201
Hyphenated Format 61010-8201

Supplemental Identifiers

UPC
0780185001008
UNII
L7T10EIP3A

Packaging Origin

Original Packager
true

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 analgesic (source: ndc)
Generic Name menthol (source: ndc)
Application Number M017 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 70 mg/L
source: ndc
Packaging
  • .059 L in 1 BOTTLE, SPRAY (61010-8201-0)
source: ndc

Packages (1)

61010-8201-0 .059 L in 1 BOTTLE, SPRAY (61010-8201-0)

Ingredients (1)

menthol (70 mg/L)

Linked Drug Pages (1)

Analgesic ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "10981167-c8a2-e068-e063-6394a90ab165", "openfda": {"upc": ["0780185001008"], "unii": ["L7T10EIP3A"], "spl_set_id": ["79e3b0e7-4ba5-4b9d-a980-5b6f18dba802"], "manufacturer_name": ["Safetec of America, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": ".059 L in 1 BOTTLE, SPRAY (61010-8201-0)", "package_ndc": "61010-8201-0", "marketing_start_date": "20180901"}], "brand_name": "Analgesic", "product_id": "61010-8201_10981167-c8a2-e068-e063-6394a90ab165", "dosage_form": "SPRAY", "product_ndc": "61010-8201", "generic_name": "menthol", "labeler_name": "Safetec of America, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Analgesic", "active_ingredients": [{"name": "MENTHOL", "strength": "70 mg/L"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20180901", "listing_expiration_date": "20261231"}