activice
Generic: menthol
Labeler: medline industries, lpDrug Facts
Product Profile
Brand Name
activice
Generic Name
menthol
Labeler
medline industries, lp
Dosage Form
LIQUID
Routes
Active Ingredients
menthol 80 g/1000g
Manufacturer
Identifiers & Regulatory
Product NDC
53329-992
Product ID
53329-992_291a13f2-c276-4f09-e063-6294a90a94d6
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M017
Listing Expiration
2026-12-31
Marketing Start
2019-03-04
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
53329992
Hyphenated Format
53329-992
Supplemental Identifiers
RxCUI
UPC
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
activice (source: ndc)
Generic Name
menthol (source: ndc)
Application Number
M017 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 80 g/1000g
Packaging
- 85 g in 1 BOTTLE, PLASTIC (53329-992-69)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "291a13f2-c276-4f09-e063-6294a90a94d6", "openfda": {"upc": ["0193489037152"], "unii": ["L7T10EIP3A"], "rxcui": ["727162", "2264041"], "spl_set_id": ["8465b443-abe9-78fb-e053-2a91aa0ac1d8"], "manufacturer_name": ["Medline Industries, LP"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "85 g in 1 BOTTLE, PLASTIC (53329-992-69)", "package_ndc": "53329-992-69", "marketing_start_date": "20190304"}], "brand_name": "ActivICE", "product_id": "53329-992_291a13f2-c276-4f09-e063-6294a90a94d6", "dosage_form": "LIQUID", "product_ndc": "53329-992", "generic_name": "menthol", "labeler_name": "Medline Industries, LP", "product_type": "HUMAN OTC DRUG", "brand_name_base": "ActivICE", "active_ingredients": [{"name": "MENTHOL", "strength": "80 g/1000g"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20190304", "listing_expiration_date": "20261231"}