coralite ultra strength pain relief

Generic: camphor menthol

Labeler: united exchange corp.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name coralite ultra strength pain relief
Generic Name camphor menthol
Labeler united exchange corp.
Dosage Form OINTMENT
Routes
TOPICAL
Active Ingredients

camphor (synthetic) 110 mg/g, menthol 110 mg/g

Manufacturer
United Exchange Corp.

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
1089831
UNII
5TJD82A1ET 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 coralite ultra strength pain relief (source: ndc)
Generic Name camphor menthol (source: ndc)
Application Number M017 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 110 mg/g
source: ndc
Packaging
  • 1 JAR in 1 CARTON (65923-532-18) / 18 g in 1 JAR
source: ndc

Packages (1)

Ingredients (2)

camphor (synthetic) (110 mg/g) menthol (110 mg/g)

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"}