medpride cold ice analgesic gel
Generic: menthol
Labeler: shield line llcDrug Facts
Product Profile
Brand Name
medpride cold ice analgesic gel
Generic Name
menthol
Labeler
shield line llc
Dosage Form
GEL
Routes
Active Ingredients
menthol 4.54 g/227g
Manufacturer
Identifiers & Regulatory
Product NDC
52410-3021
Product ID
52410-3021_3c6ee220-9e8e-649b-e063-6394a90a3e16
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
524103021
Hyphenated Format
52410-3021
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
medpride 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 (52410-3021-2)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "3c6ee220-9e8e-649b-e063-6394a90a3e16", "openfda": {"unii": ["L7T10EIP3A"], "rxcui": ["311502"], "spl_set_id": ["860a2c86-b240-4e0e-e053-2a91aa0a333a"], "manufacturer_name": ["SHIELD LINE LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "227 g in 1 JAR (52410-3021-2)", "package_ndc": "52410-3021-2", "marketing_start_date": "20190408"}], "brand_name": "MedPride Cold Ice Analgesic Gel", "product_id": "52410-3021_3c6ee220-9e8e-649b-e063-6394a90a3e16", "dosage_form": "GEL", "product_ndc": "52410-3021", "generic_name": "Menthol", "labeler_name": "SHIELD LINE LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "MedPride 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"}