kens pain and arthritis formula

Generic: menthol

Labeler: eezaway relief inc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name kens pain and arthritis formula
Generic Name menthol
Labeler eezaway relief inc
Dosage Form LIQUID
Routes
TOPICAL
Active Ingredients

menthol, unspecified form 2.75 g/100mL

Manufacturer
Eezaway Relief Inc

Identifiers & Regulatory

Product NDC 69678-143
Product ID 69678-143_c01c4dab-9263-43d7-88dd-5df72403f96c
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M017
Listing Expiration 2026-12-31
Marketing Start 2024-03-05

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 69678143
Hyphenated Format 69678-143

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 kens pain and arthritis formula (source: ndc)
Generic Name menthol (source: ndc)
Application Number M017 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 2.75 g/100mL
source: ndc
Packaging
  • 88 mL in 1 BOTTLE (69678-143-03)
source: ndc

Packages (1)

69678-143-03 88 mL in 1 BOTTLE (69678-143-03)

Ingredients (1)

menthol, unspecified form (2.75 g/100mL)

Linked Drug Pages (1)

KENS PAIN AND ARTHRITIS FORMULA ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "c01c4dab-9263-43d7-88dd-5df72403f96c", "openfda": {"unii": ["L7T10EIP3A"], "spl_set_id": ["35834473-3ad5-41ec-a110-e742aa7e2ee4"], "manufacturer_name": ["Eezaway Relief Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "88 mL in 1 BOTTLE (69678-143-03)", "package_ndc": "69678-143-03", "marketing_start_date": "20240305"}], "brand_name": "KENS PAIN AND ARTHRITIS FORMULA", "product_id": "69678-143_c01c4dab-9263-43d7-88dd-5df72403f96c", "dosage_form": "LIQUID", "product_ndc": "69678-143", "generic_name": "MENTHOL", "labeler_name": "Eezaway Relief Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "KENS PAIN AND ARTHRITIS FORMULA", "active_ingredients": [{"name": "MENTHOL, UNSPECIFIED FORM", "strength": "2.75 g/100mL"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240305", "listing_expiration_date": "20261231"}