cold ice analgesic gel
Generic: menthol
Labeler: dabur india limitedDrug Facts
Product Profile
Brand Name
cold ice analgesic gel
Generic Name
menthol
Labeler
dabur india limited
Dosage Form
GEL
Routes
Active Ingredients
menthol 4.54 g/227g
Manufacturer
Identifiers & Regulatory
Product NDC
68747-3021
Product ID
68747-3021_22914641-7f94-5d16-e063-6394a90a455e
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M017
Listing Expiration
2026-12-31
Marketing Start
2019-04-08
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
687473021
Hyphenated Format
68747-3021
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
cold ice analgesic gel (source: ndc)
Generic Name
menthol (source: ndc)
Application Number
M017 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 4.54 g/227g
Packaging
- 227 g in 1 JAR (68747-3021-2)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "22914641-7f94-5d16-e063-6394a90a455e", "openfda": {"unii": ["L7T10EIP3A"], "rxcui": ["311502"], "spl_set_id": ["22915b2f-5f76-3e38-e063-6394a90a07b4"], "manufacturer_name": ["Dabur India Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "227 g in 1 JAR (68747-3021-2)", "package_ndc": "68747-3021-2", "marketing_start_date": "20190408"}], "brand_name": "Cold Ice Analgesic Gel", "product_id": "68747-3021_22914641-7f94-5d16-e063-6394a90a455e", "dosage_form": "GEL", "product_ndc": "68747-3021", "generic_name": "Menthol", "labeler_name": "Dabur India Limited", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Cold Ice Analgesic Gel", "active_ingredients": [{"name": "MENTHOL", "strength": "4.54 g/227g"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20190408", "listing_expiration_date": "20261231"}