dirt pain relieving gel
Generic: menthol
Labeler: purivitae, llcDrug Facts
Product Profile
Brand Name
dirt pain relieving gel
Generic Name
menthol
Labeler
purivitae, llc
Dosage Form
GEL
Routes
Active Ingredients
menthol 40 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
83067-463
Product ID
83067-463_097705c5-f169-19a5-e063-6294a90acfaf
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M017
Listing Expiration
2026-12-31
Marketing Start
2023-10-03
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
83067463
Hyphenated Format
83067-463
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
dirt pain relieving gel (source: ndc)
Generic Name
menthol (source: ndc)
Application Number
M017 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 40 mg/mL
Packaging
- 88 mL in 1 BOTTLE (83067-463-00)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "097705c5-f169-19a5-e063-6294a90acfaf", "openfda": {"unii": ["L7T10EIP3A"], "rxcui": ["415974"], "spl_set_id": ["e43e2cbd-d114-4b11-8baf-7a775881cd97"], "manufacturer_name": ["PURIVITAE, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "88 mL in 1 BOTTLE (83067-463-00)", "package_ndc": "83067-463-00", "marketing_start_date": "20231003"}], "brand_name": "DIRT Pain Relieving Gel", "product_id": "83067-463_097705c5-f169-19a5-e063-6294a90acfaf", "dosage_form": "GEL", "product_ndc": "83067-463", "generic_name": "MENTHOL", "labeler_name": "PURIVITAE, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "DIRT Pain Relieving Gel", "active_ingredients": [{"name": "MENTHOL", "strength": "40 mg/mL"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20231003", "listing_expiration_date": "20261231"}