analgesic

Generic: menthol

Labeler: safetec of america, inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH NOT FINAL Inactive Finished

Drug Facts

Product Profile

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

menthol 70 mg/L

Manufacturer
Safetec of America, Inc.

Identifiers & Regulatory

Product NDC 61010-8202
Product ID 61010-8202_a4cdd5eb-fbda-4f99-b737-452a1487adfd
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH NOT FINAL
Application Number part348
Listing Expiration 2026-12-31
Marketing Start 2018-09-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 610108202
Hyphenated Format 61010-8202

Supplemental Identifiers

UPC
0780185001015
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 part348 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 70 mg/L
source: ndc
Packaging
  • .088 L in 1 BOTTLE, WITH APPLICATOR (61010-8202-0)
source: ndc

Packages (1)

61010-8202-0 .088 L in 1 BOTTLE, WITH APPLICATOR (61010-8202-0)

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": "a4cdd5eb-fbda-4f99-b737-452a1487adfd", "openfda": {"upc": ["0780185001015"], "unii": ["L7T10EIP3A"], "spl_set_id": ["a90266d4-1e71-4805-aeca-6f8ed45135bb"], "manufacturer_name": ["Safetec of America, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": ".088 L in 1 BOTTLE, WITH APPLICATOR (61010-8202-0)", "package_ndc": "61010-8202-0", "marketing_start_date": "20180901"}], "brand_name": "Analgesic", "product_id": "61010-8202_a4cdd5eb-fbda-4f99-b737-452a1487adfd", "dosage_form": "GEL", "product_ndc": "61010-8202", "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": "part348", "marketing_category": "OTC MONOGRAPH NOT FINAL", "marketing_start_date": "20180901", "listing_expiration_date": "20261231"}