gems menthol eucalyptus
Generic: menthol
Labeler: riclan s.a.Drug Facts
Product Profile
Brand Name
gems menthol eucalyptus
Generic Name
menthol
Labeler
riclan s.a.
Dosage Form
LOZENGE
Routes
Active Ingredients
menthol 8.4 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
71165-173
Product ID
71165-173_9d84d02f-05d4-4afc-9a57-fd281a8e1b01
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M012
Listing Expiration
2026-12-31
Marketing Start
2021-09-13
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
71165173
Hyphenated Format
71165-173
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
gems menthol eucalyptus (source: ndc)
Generic Name
menthol (source: ndc)
Application Number
M012 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 8.4 mg/1
Packaging
- 9 LOZENGE in 1 PACKAGE (71165-173-02)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "9d84d02f-05d4-4afc-9a57-fd281a8e1b01", "openfda": {"upc": ["0371165173022"], "unii": ["L7T10EIP3A"], "rxcui": ["311512"], "spl_set_id": ["853254be-2d3b-46a8-97b9-8532f771a828"], "manufacturer_name": ["Riclan S.A."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "9 LOZENGE in 1 PACKAGE (71165-173-02)", "package_ndc": "71165-173-02", "marketing_start_date": "20210913"}], "brand_name": "Gems Menthol Eucalyptus", "product_id": "71165-173_9d84d02f-05d4-4afc-9a57-fd281a8e1b01", "dosage_form": "LOZENGE", "product_ndc": "71165-173", "generic_name": "Menthol", "labeler_name": "Riclan S.A.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Gems", "brand_name_suffix": "Menthol Eucalyptus", "active_ingredients": [{"name": "MENTHOL", "strength": "8.4 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20210913", "listing_expiration_date": "20261231"}