pharmacys prescription analgesic gel

Generic: menthol

Labeler: american consumer products corp
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name pharmacys prescription analgesic gel
Generic Name menthol
Labeler american consumer products corp
Dosage Form GEL
Routes
TOPICAL
Active Ingredients

menthol 1 g/100g

Manufacturer
American Consumer Products Corp

Identifiers & Regulatory

Product NDC 72197-001
Product ID 72197-001_2c69ab76-e3d1-1436-e063-6294a90aa515
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2018-08-31

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72197001
Hyphenated Format 72197-001

Supplemental Identifiers

RxCUI
1039043
UPC
0757437700057
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 pharmacys prescription analgesic gel (source: ndc)
Generic Name menthol (source: ndc)
Application Number M012 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 1 g/100g
source: ndc
Packaging
  • 227 g in 1 BOTTLE, PLASTIC (72197-001-08)
source: ndc

Packages (1)

72197-001-08 227 g in 1 BOTTLE, PLASTIC (72197-001-08)

Ingredients (1)

menthol (1 g/100g)

Linked Drug Pages (1)

Pharmacys Prescription Analgesic Gel ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "2c69ab76-e3d1-1436-e063-6294a90aa515", "openfda": {"upc": ["0757437700057"], "unii": ["L7T10EIP3A"], "rxcui": ["1039043"], "spl_set_id": ["6f0725f2-833f-f3a0-e053-2a91aa0a3911"], "manufacturer_name": ["American Consumer Products Corp"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "227 g in 1 BOTTLE, PLASTIC (72197-001-08)", "package_ndc": "72197-001-08", "marketing_start_date": "20180831"}], "brand_name": "Pharmacys Prescription Analgesic Gel", "product_id": "72197-001_2c69ab76-e3d1-1436-e063-6294a90aa515", "dosage_form": "GEL", "product_ndc": "72197-001", "generic_name": "Menthol", "labeler_name": "American Consumer Products Corp", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Pharmacys Prescription Analgesic Gel", "active_ingredients": [{"name": "MENTHOL", "strength": "1 g/100g"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20180831", "listing_expiration_date": "20261231"}