biofreeze overnight roll-on
Generic: menthol
Labeler: rb health (us) llcDrug Facts
Product Profile
Brand Name
biofreeze overnight roll-on
Generic Name
menthol
Labeler
rb health (us) llc
Dosage Form
GEL
Routes
Active Ingredients
menthol 40 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
59316-207
Product ID
59316-207_2a468180-88eb-8045-e063-6394a90ac816
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M017
Listing Expiration
2026-12-31
Marketing Start
2023-03-16
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
59316207
Hyphenated Format
59316-207
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
biofreeze overnight roll-on (source: ndc)
Generic Name
menthol (source: ndc)
Application Number
M017 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 40 mg/mL
Packaging
- 74 mL in 1 BOTTLE (59316-207-14)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "2a468180-88eb-8045-e063-6394a90ac816", "openfda": {"unii": ["L7T10EIP3A"], "rxcui": ["415974", "1111683"], "spl_set_id": ["f67d7b7a-8922-73f6-e053-2995a90a2e80"], "manufacturer_name": ["RB Health (US) LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "74 mL in 1 BOTTLE (59316-207-14)", "package_ndc": "59316-207-14", "marketing_start_date": "20230316"}], "brand_name": "Biofreeze Overnight Roll-on", "product_id": "59316-207_2a468180-88eb-8045-e063-6394a90ac816", "dosage_form": "GEL", "product_ndc": "59316-207", "generic_name": "Menthol", "labeler_name": "RB Health (US) LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Biofreeze Overnight Roll-on", "active_ingredients": [{"name": "MENTHOL", "strength": "40 mg/mL"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20230316", "listing_expiration_date": "20261231"}