uriflex fast acting analgesic pain relief
Generic: menthol
Labeler: rejuvica llcDrug Facts
Product Profile
Brand Name
uriflex fast acting analgesic pain relief
Generic Name
menthol
Labeler
rejuvica llc
Dosage Form
CREAM
Routes
Active Ingredients
menthol 45 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
73168-004
Product ID
73168-004_09751fc7-6657-c196-e063-6294a90a4a57
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M017
Listing Expiration
2026-12-31
Marketing Start
2019-05-20
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
73168004
Hyphenated Format
73168-004
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
uriflex fast acting analgesic pain relief (source: ndc)
Generic Name
menthol (source: ndc)
Application Number
M017 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 45 mg/mL
Packaging
- 118 mL in 1 JAR (73168-004-00)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "09751fc7-6657-c196-e063-6294a90a4a57", "openfda": {"unii": ["L7T10EIP3A"], "rxcui": ["2171392"], "spl_set_id": ["fb78f705-b838-461d-b42c-8c98d3ca5d09"], "manufacturer_name": ["Rejuvica LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "118 mL in 1 JAR (73168-004-00)", "package_ndc": "73168-004-00", "marketing_start_date": "20190520"}], "brand_name": "URIFLEX Fast Acting Analgesic Pain Relief", "product_id": "73168-004_09751fc7-6657-c196-e063-6294a90a4a57", "dosage_form": "CREAM", "product_ndc": "73168-004", "generic_name": "MENTHOL", "labeler_name": "Rejuvica LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "URIFLEX Fast Acting Analgesic Pain Relief", "active_ingredients": [{"name": "MENTHOL", "strength": "45 mg/mL"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20190520", "listing_expiration_date": "20261231"}