premieres pain
Generic: menthol
Labeler: premiere enterprisesDrug Facts
Product Profile
Brand Name
premieres pain
Generic Name
menthol
Labeler
premiere enterprises
Dosage Form
SPRAY
Routes
Active Ingredients
menthol 7 g/100mL
Manufacturer
Identifiers & Regulatory
Product NDC
32472-102
Product ID
32472-102_46a6f042-1930-0688-e063-6294a90ae162
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M017
Listing Expiration
2026-12-31
Marketing Start
2011-01-12
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
32472102
Hyphenated Format
32472-102
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
premieres pain (source: ndc)
Generic Name
menthol (source: ndc)
Application Number
M017 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 7 g/100mL
Packaging
- 88 mL in 1 BOTTLE (32472-102-03)
Packages (1)
Ingredients (1)
Linked Drug Pages (3)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "46a6f042-1930-0688-e063-6294a90ae162", "openfda": {"upc": ["0783239003072"], "unii": ["L7T10EIP3A"], "rxcui": ["1086713"], "spl_set_id": ["35ff19df-4cc4-4fce-bd30-d87d835e0e26"], "manufacturer_name": ["Premiere Enterprises"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "88 mL in 1 BOTTLE (32472-102-03)", "package_ndc": "32472-102-03", "marketing_start_date": "20110112"}], "brand_name": "PREMIERES PAIN", "product_id": "32472-102_46a6f042-1930-0688-e063-6294a90ae162", "dosage_form": "SPRAY", "product_ndc": "32472-102", "generic_name": "menthol", "labeler_name": "Premiere Enterprises", "product_type": "HUMAN OTC DRUG", "brand_name_base": "PREMIERES PAIN", "active_ingredients": [{"name": "MENTHOL", "strength": "7 g/100mL"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20110112", "listing_expiration_date": "20261231"}