sunset cooling pain relief roll-on
Generic: menthol
Labeler: sunset novelties, incDrug Facts
Product Profile
Brand Name
sunset cooling pain relief roll-on
Generic Name
menthol
Labeler
sunset novelties, inc
Dosage Form
GEL
Routes
Active Ingredients
menthol 4 g/100mL
Manufacturer
Identifiers & Regulatory
Product NDC
72937-631
Product ID
72937-631_45037bca-b20f-00c2-e063-6394a90a3607
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M017
Listing Expiration
2026-12-31
Marketing Start
2025-12-01
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
72937631
Hyphenated Format
72937-631
Supplemental Identifiers
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
sunset cooling pain relief roll-on (source: ndc)
Generic Name
menthol (source: ndc)
Application Number
M017 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 4 g/100mL
Packaging
- 89 mL in 1 BOTTLE (72937-631-03)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "45037bca-b20f-00c2-e063-6394a90a3607", "openfda": {"unii": ["L7T10EIP3A"], "spl_set_id": ["45037bc1-aa03-11ae-e063-6294a90a6c96"], "manufacturer_name": ["SUNSET NOVELTIES, INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "89 mL in 1 BOTTLE (72937-631-03)", "package_ndc": "72937-631-03", "marketing_start_date": "20251201"}], "brand_name": "SUNSET COOLING PAIN RELIEF ROLL-ON", "product_id": "72937-631_45037bca-b20f-00c2-e063-6394a90a3607", "dosage_form": "GEL", "product_ndc": "72937-631", "generic_name": "MENTHOL", "labeler_name": "SUNSET NOVELTIES, INC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "SUNSET COOLING PAIN RELIEF ROLL-ON", "active_ingredients": [{"name": "MENTHOL", "strength": "4 g/100mL"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20251201", "listing_expiration_date": "20261231"}