menthol cough drops
Generic: menthol
Labeler: target corporation inc.Drug Facts
Product Profile
Brand Name
menthol cough drops
Generic Name
menthol
Labeler
target corporation inc.
Dosage Form
PASTILLE
Routes
Active Ingredients
menthol 5.8 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
82442-001
Product ID
82442-001_2c9f047d-e703-dff0-e063-6294a90a1c50
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M012
Listing Expiration
2026-12-31
Marketing Start
2022-10-18
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
82442001
Hyphenated Format
82442-001
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
menthol cough drops (source: ndc)
Generic Name
menthol (source: ndc)
Application Number
M012 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 5.8 mg/1
Packaging
- 80 PASTILLE in 1 BAG (82442-001-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (2)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2c9f047d-e703-dff0-e063-6294a90a1c50", "openfda": {"upc": ["0850017715448"], "unii": ["L7T10EIP3A"], "rxcui": ["476973"], "spl_set_id": ["eb4c2c3f-91d7-e4c6-e053-2a95a90a4e8a"], "manufacturer_name": ["Target Corporation Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "80 PASTILLE in 1 BAG (82442-001-01)", "package_ndc": "82442-001-01", "marketing_start_date": "20221024"}], "brand_name": "Menthol Cough Drops", "product_id": "82442-001_2c9f047d-e703-dff0-e063-6294a90a1c50", "dosage_form": "PASTILLE", "product_ndc": "82442-001", "generic_name": "Menthol", "labeler_name": "Target Corporation Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Menthol Cough Drops", "active_ingredients": [{"name": "MENTHOL", "strength": "5.8 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20221018", "listing_expiration_date": "20261231"}