ultra relief

Generic: menthol, camphor

Labeler: chemco corporation
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name ultra relief
Generic Name menthol, camphor
Labeler chemco corporation
Dosage Form GEL
Routes
TOPICAL
Active Ingredients

camphor (synthetic) 3 g/100g, menthol 6 g/100g

Manufacturer
CHEMCO CORPORATION

Identifiers & Regulatory

Product NDC 49283-578
Product ID 49283-578_48e9bcf4-0751-7b3f-e063-6294a90ac649
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M017
Listing Expiration 2027-12-31
Marketing Start 2026-01-15

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 49283578
Hyphenated Format 49283-578

Supplemental Identifiers

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 ultra relief (source: ndc)
Generic Name menthol, camphor (source: ndc)
Application Number M017 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 3 g/100g
  • 6 g/100g
source: ndc
Packaging
  • 113 g in 1 BOTTLE, PUMP (49283-578-04)
source: ndc

Packages (1)

49283-578-04 113 g in 1 BOTTLE, PUMP (49283-578-04)

Ingredients (2)

camphor (synthetic) (3 g/100g) menthol (6 g/100g)

Linked Drug Pages (1)

ULTRA RELIEF ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "48e9bcf4-0751-7b3f-e063-6294a90ac649", "openfda": {"unii": ["5TJD82A1ET", "L7T10EIP3A"], "spl_set_id": ["48ea80cf-af54-ce5f-e063-6394a90ac493"], "manufacturer_name": ["CHEMCO CORPORATION"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "113 g in 1 BOTTLE, PUMP (49283-578-04)", "package_ndc": "49283-578-04", "marketing_start_date": "20260115"}], "brand_name": "ULTRA RELIEF", "product_id": "49283-578_48e9bcf4-0751-7b3f-e063-6294a90ac649", "dosage_form": "GEL", "product_ndc": "49283-578", "generic_name": "MENTHOL, CAMPHOR", "labeler_name": "CHEMCO CORPORATION", "product_type": "HUMAN OTC DRUG", "brand_name_base": "ULTRA RELIEF", "active_ingredients": [{"name": "CAMPHOR (SYNTHETIC)", "strength": "3 g/100g"}, {"name": "MENTHOL", "strength": "6 g/100g"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20260115", "listing_expiration_date": "20271231"}