vapor shower
Generic: menthol
Labeler: xiamen kang zhongyuan biotechnology co., ltd.Drug Facts
Product Profile
Brand Name
vapor shower
Generic Name
menthol
Labeler
xiamen kang zhongyuan biotechnology co., ltd.
Dosage Form
TABLET
Routes
Active Ingredients
menthol .45 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
83698-005
Product ID
83698-005_2cf2f363-2b77-f131-e063-6394a90a1d7a
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M012
Listing Expiration
2026-12-31
Marketing Start
2025-01-01
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
83698005
Hyphenated Format
83698-005
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
vapor shower (source: ndc)
Generic Name
menthol (source: ndc)
Application Number
M012 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .45 mg/1
Packaging
- 10 TABLET in 1 PACKAGE (83698-005-10)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "2cf2f363-2b77-f131-e063-6394a90a1d7a", "openfda": {"unii": ["L7T10EIP3A"], "spl_set_id": ["2cf2f35b-5d59-e3ff-e063-6294a90a9b45"], "manufacturer_name": ["Xiamen Kang Zhongyuan Biotechnology Co., Ltd."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET in 1 PACKAGE (83698-005-10)", "package_ndc": "83698-005-10", "marketing_start_date": "20250101"}], "brand_name": "Vapor Shower", "product_id": "83698-005_2cf2f363-2b77-f131-e063-6394a90a1d7a", "dosage_form": "TABLET", "product_ndc": "83698-005", "generic_name": "Menthol", "labeler_name": "Xiamen Kang Zhongyuan Biotechnology Co., Ltd.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Vapor Shower", "active_ingredients": [{"name": "MENTHOL", "strength": ".45 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250101", "listing_expiration_date": "20261231"}