point relief cold spot pain relieving roll-on

Generic: menthol

Labeler: fabrication enterprises
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name point relief cold spot pain relieving roll-on
Generic Name menthol
Labeler fabrication enterprises
Dosage Form LIQUID
Routes
TOPICAL
Active Ingredients

menthol 140 mg/mL

Manufacturer
Fabrication Enterprises

Identifiers & Regulatory

Product NDC 51452-037
Product ID 51452-037_0973b73d-5dde-0986-e063-6294a90a5917
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M017
Listing Expiration 2026-12-31
Marketing Start 2019-04-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 51452037
Hyphenated Format 51452-037

Supplemental Identifiers

RxCUI
2121681 2121685
UPC
0714905024701
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 point relief cold spot pain relieving roll-on (source: ndc)
Generic Name menthol (source: ndc)
Application Number M017 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 140 mg/mL
source: ndc
Packaging
  • 90 mL in 1 CONTAINER (51452-037-06)
source: ndc

Packages (1)

51452-037-06 90 mL in 1 CONTAINER (51452-037-06)

Ingredients (1)

menthol (140 mg/mL)

Linked Drug Pages (1)

Point Relief cold Spot Pain Relieving roll-on ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "0973b73d-5dde-0986-e063-6294a90a5917", "openfda": {"upc": ["0714905024701"], "unii": ["L7T10EIP3A"], "rxcui": ["2121681", "2121685"], "spl_set_id": ["3f1db0ad-aaa8-4e14-9349-45057e0fb4a6"], "manufacturer_name": ["Fabrication Enterprises"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 mL in 1 CONTAINER (51452-037-06)", "package_ndc": "51452-037-06", "marketing_start_date": "20190401"}], "brand_name": "Point Relief cold Spot Pain Relieving roll-on", "product_id": "51452-037_0973b73d-5dde-0986-e063-6294a90a5917", "dosage_form": "LIQUID", "product_ndc": "51452-037", "generic_name": "MENTHOL", "labeler_name": "Fabrication Enterprises", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Point Relief cold Spot Pain Relieving roll-on", "active_ingredients": [{"name": "MENTHOL", "strength": "140 mg/mL"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20190401", "listing_expiration_date": "20261231"}