ice muscle rub leon m.c
Generic: menthol
Labeler: southern sales & service, inc.Drug Facts
Product Profile
Brand Name
ice muscle rub leon m.c
Generic Name
menthol
Labeler
southern sales & service, inc.
Dosage Form
GEL
Routes
Active Ingredients
menthol .02 g/g
Manufacturer
Identifiers & Regulatory
Product NDC
69822-103
Product ID
69822-103_0b57d91e-06ca-37f8-e063-6294a90a6515
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M017
Listing Expiration
2026-12-31
Marketing Start
2015-01-04
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
69822103
Hyphenated Format
69822-103
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
ice muscle rub leon m.c (source: ndc)
Generic Name
menthol (source: ndc)
Application Number
M017 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .02 g/g
Packaging
- 227 g in 1 TUBE (69822-103-08)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "0b57d91e-06ca-37f8-e063-6294a90a6515", "openfda": {"unii": ["L7T10EIP3A"], "rxcui": ["311502"], "spl_set_id": ["4efaf347-7406-4690-8005-e7cf2e3d4222"], "manufacturer_name": ["Southern Sales & Service, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "227 g in 1 TUBE (69822-103-08)", "package_ndc": "69822-103-08", "marketing_start_date": "20150104"}], "brand_name": "ICE MUSCLE RUB Leon M.C", "product_id": "69822-103_0b57d91e-06ca-37f8-e063-6294a90a6515", "dosage_form": "GEL", "product_ndc": "69822-103", "generic_name": "Menthol", "labeler_name": "Southern Sales & Service, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "ICE MUSCLE RUB Leon M.C", "active_ingredients": [{"name": "MENTHOL", "strength": ".02 g/g"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20150104", "listing_expiration_date": "20261231"}