coralite cold and hot
Generic: menthol
Labeler: united exchange corp.Drug Facts
Product Profile
Brand Name
coralite cold and hot
Generic Name
menthol
Labeler
united exchange corp.
Dosage Form
PATCH
Routes
Active Ingredients
menthol 210 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
65923-214
Product ID
65923-214_41c7473a-cea8-3353-e063-6294a90a5e41
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M017
Listing Expiration
2026-12-31
Marketing Start
2023-09-26
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
65923214
Hyphenated Format
65923-214
Supplemental Identifiers
RxCUI
UPC
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
coralite cold and hot (source: ndc)
Generic Name
menthol (source: ndc)
Application Number
M017 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 210 mg/1
Packaging
- 1 PATCH in 1 POUCH (65923-214-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "41c7473a-cea8-3353-e063-6294a90a5e41", "openfda": {"upc": ["0780707902141"], "unii": ["L7T10EIP3A"], "rxcui": ["1010823"], "spl_set_id": ["064a6149-a0e2-8a73-e063-6394a90a7953"], "manufacturer_name": ["United Exchange Corp."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 PATCH in 1 POUCH (65923-214-01)", "package_ndc": "65923-214-01", "marketing_start_date": "20230926"}], "brand_name": "Coralite Cold and Hot", "product_id": "65923-214_41c7473a-cea8-3353-e063-6294a90a5e41", "dosage_form": "PATCH", "product_ndc": "65923-214", "generic_name": "Menthol", "labeler_name": "United Exchange Corp.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Coralite Cold and Hot", "active_ingredients": [{"name": "MENTHOL", "strength": "210 mg/1"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20230926", "listing_expiration_date": "20261231"}