mineral ice pain relieving

Generic: menthol

Labeler: crown laboratories
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name mineral ice pain relieving
Generic Name menthol
Labeler crown laboratories
Dosage Form GEL
Routes
TOPICAL
Active Ingredients

menthol 20 mg/g

Manufacturer
Crown Laboratories

Identifiers & Regulatory

Product NDC 0316-0226
Product ID 0316-0226_4833e9dd-2f42-f6d5-e063-6394a90a1b0a
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M017
Listing Expiration 2027-12-31
Marketing Start 2011-11-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 03160226
Hyphenated Format 0316-0226

Supplemental Identifiers

RxCUI
311502 692869
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 mineral ice pain relieving (source: ndc)
Generic Name menthol (source: ndc)
Application Number M017 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/g
source: ndc
Packaging
  • 226.8 g in 1 JAR (0316-0226-08)
  • 453.6 g in 1 JAR (0316-0226-16)
source: ndc

Packages (2)

Ingredients (1)

menthol (20 mg/g)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "4833e9dd-2f42-f6d5-e063-6394a90a1b0a", "openfda": {"unii": ["L7T10EIP3A"], "rxcui": ["311502", "692869"], "spl_set_id": ["7b30076a-0af6-2f74-e053-2a91aa0ae08d"], "manufacturer_name": ["Crown Laboratories"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "226.8 g in 1 JAR (0316-0226-08)", "package_ndc": "0316-0226-08", "marketing_start_date": "20181201"}, {"sample": false, "description": "453.6 g in 1 JAR (0316-0226-16)", "package_ndc": "0316-0226-16", "marketing_start_date": "20181201"}], "brand_name": "Mineral Ice Pain Relieving", "product_id": "0316-0226_4833e9dd-2f42-f6d5-e063-6394a90a1b0a", "dosage_form": "GEL", "product_ndc": "0316-0226", "generic_name": "Menthol", "labeler_name": "Crown Laboratories", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mineral Ice", "brand_name_suffix": "Pain Relieving", "active_ingredients": [{"name": "MENTHOL", "strength": "20 mg/g"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20111101", "listing_expiration_date": "20271231"}