coralite ultra strength pain relief
Generic: camphor menthol
Labeler: united exchange corp.Drug Facts
Product Profile
Brand Name
coralite ultra strength pain relief
Generic Name
camphor menthol
Labeler
united exchange corp.
Dosage Form
OINTMENT
Routes
Active Ingredients
camphor (synthetic) 110 mg/g, menthol 110 mg/g
Manufacturer
Identifiers & Regulatory
Product NDC
65923-532
Product ID
65923-532_425530d6-e8ea-f05c-e063-6294a90aff39
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M017
Listing Expiration
2026-12-31
Marketing Start
2014-10-15
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
65923532
Hyphenated Format
65923-532
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
coralite ultra strength pain relief (source: ndc)
Generic Name
camphor menthol (source: ndc)
Application Number
M017 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 110 mg/g
Packaging
- 1 JAR in 1 CARTON (65923-532-18) / 18 g in 1 JAR
Packages (1)
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "425530d6-e8ea-f05c-e063-6294a90aff39", "openfda": {"unii": ["5TJD82A1ET", "L7T10EIP3A"], "rxcui": ["1089831"], "spl_set_id": ["44ecf959-cc07-4adc-a500-075b2ee69548"], "manufacturer_name": ["United Exchange Corp."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 JAR in 1 CARTON (65923-532-18) / 18 g in 1 JAR", "package_ndc": "65923-532-18", "marketing_start_date": "20171213"}], "brand_name": "Coralite Ultra Strength Pain Relief", "product_id": "65923-532_425530d6-e8ea-f05c-e063-6294a90aff39", "dosage_form": "OINTMENT", "product_ndc": "65923-532", "generic_name": "Camphor Menthol", "labeler_name": "United Exchange Corp.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Coralite Ultra Strength Pain Relief", "active_ingredients": [{"name": "CAMPHOR (SYNTHETIC)", "strength": "110 mg/g"}, {"name": "MENTHOL", "strength": "110 mg/g"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20141015", "listing_expiration_date": "20261231"}