rocksauce icy cold pain relief
Generic: menthol
Labeler: implus footcare, llcDrug Facts
Product Profile
Brand Name
rocksauce icy cold pain relief
Generic Name
menthol
Labeler
implus footcare, llc
Dosage Form
GEL
Routes
Active Ingredients
menthol 8.3 g/88.5mL
Manufacturer
Identifiers & Regulatory
Product NDC
81683-003
Product ID
81683-003_3239950d-8958-aaaa-e063-6394a90a8fa2
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M017
Listing Expiration
2026-12-31
Marketing Start
2021-03-18
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
81683003
Hyphenated Format
81683-003
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
rocksauce icy cold pain relief (source: ndc)
Generic Name
menthol (source: ndc)
Application Number
M017 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 8.3 g/88.5mL
Packaging
- 88.5 mL in 1 BOTTLE (81683-003-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "3239950d-8958-aaaa-e063-6394a90a8fa2", "openfda": {"unii": ["L7T10EIP3A"], "spl_set_id": ["bd4fdff1-9174-31c2-e053-2a95a90a749f"], "manufacturer_name": ["Implus Footcare, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "88.5 mL in 1 BOTTLE (81683-003-01)", "package_ndc": "81683-003-01", "marketing_start_date": "20210318"}], "brand_name": "RockSauce ICY COLD PAIN RELIEF", "product_id": "81683-003_3239950d-8958-aaaa-e063-6394a90a8fa2", "dosage_form": "GEL", "product_ndc": "81683-003", "generic_name": "Menthol", "labeler_name": "Implus Footcare, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "RockSauce ICY COLD PAIN RELIEF", "active_ingredients": [{"name": "MENTHOL", "strength": "8.3 g/88.5mL"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20210318", "listing_expiration_date": "20261231"}