ultra strength pain relief gel

Generic: menthol

Labeler: telebrands corp
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name ultra strength pain relief gel
Generic Name menthol
Labeler telebrands corp
Dosage Form LOTION
Routes
TOPICAL
Active Ingredients

menthol 8 g/100g

Manufacturer
TELEBRANDS CORP

Identifiers & Regulatory

Product NDC 73287-023
Product ID 73287-023_275b89dc-566d-3bc1-e063-6394a90a9cad
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M017
Listing Expiration 2026-12-31
Marketing Start 2022-02-28

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 73287023
Hyphenated Format 73287-023

Supplemental Identifiers

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 ultra strength pain relief gel (source: ndc)
Generic Name menthol (source: ndc)
Application Number M017 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 8 g/100g
source: ndc
Packaging
  • 1 APPLICATOR in 1 CARTON (73287-023-01) / 71 g in 1 APPLICATOR
source: ndc

Packages (1)

73287-023-01 1 APPLICATOR in 1 CARTON (73287-023-01) / 71 g in 1 APPLICATOR

Ingredients (1)

menthol (8 g/100g)

Linked Drug Pages (1)

Ultra Strength Pain Relief Gel ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "275b89dc-566d-3bc1-e063-6394a90a9cad", "openfda": {"unii": ["L7T10EIP3A"], "spl_set_id": ["d91b2e09-550e-4968-e053-2995a90ae323"], "manufacturer_name": ["TELEBRANDS CORP"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 APPLICATOR in 1 CARTON (73287-023-01)  / 71 g in 1 APPLICATOR", "package_ndc": "73287-023-01", "marketing_start_date": "20220228"}], "brand_name": "Ultra Strength Pain Relief Gel", "product_id": "73287-023_275b89dc-566d-3bc1-e063-6394a90a9cad", "dosage_form": "LOTION", "product_ndc": "73287-023", "generic_name": "Menthol", "labeler_name": "TELEBRANDS CORP", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Ultra Strength Pain Relief Gel", "active_ingredients": [{"name": "MENTHOL", "strength": "8 g/100g"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20220228", "listing_expiration_date": "20261231"}