invigo flex pain relief gel
Generic: menthol
Labeler: wynnpharm inc.Drug Facts
Product Profile
Brand Name
invigo flex pain relief gel
Generic Name
menthol
Labeler
wynnpharm inc.
Dosage Form
GEL
Routes
Active Ingredients
menthol 30 mg/g
Manufacturer
Identifiers & Regulatory
Product NDC
35324-276
Product ID
35324-276_09d70e71-d1be-2749-e063-6294a90abd05
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M017
Listing Expiration
2026-12-31
Marketing Start
2022-02-15
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
35324276
Hyphenated Format
35324-276
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
invigo flex pain relief gel (source: ndc)
Generic Name
menthol (source: ndc)
Application Number
M017 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 30 mg/g
Packaging
- 1 TUBE in 1 BOX (35324-276-00) / 75 g in 1 TUBE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "09d70e71-d1be-2749-e063-6294a90abd05", "openfda": {"unii": ["L7T10EIP3A"], "rxcui": ["259150"], "spl_set_id": ["909e1d8c-c517-4d6a-8682-894f042c00f8"], "manufacturer_name": ["WYNNPHARM INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 BOX (35324-276-00) / 75 g in 1 TUBE", "package_ndc": "35324-276-00", "marketing_start_date": "20220215"}], "brand_name": "INVIGO FLEX Pain Relief Gel", "product_id": "35324-276_09d70e71-d1be-2749-e063-6294a90abd05", "dosage_form": "GEL", "product_ndc": "35324-276", "generic_name": "MENTHOL", "labeler_name": "WYNNPHARM INC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "INVIGO FLEX Pain Relief Gel", "active_ingredients": [{"name": "MENTHOL", "strength": "30 mg/g"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20220215", "listing_expiration_date": "20261231"}