NDC 44237-008 Herbion Naturals Honey-lemon Cough Drops
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 44237 - Herbion Pakistan (pvt.) Ltd.
- 44237-008 - Herbion Naturals
Product Characteristics
LEMON (C73396)
Product Packages
NDC Code 44237-008-18
Package Description: 2 BLISTER PACK in 1 CARTON / 9 LOZENGE in 1 BLISTER PACK
Product Details
What is NDC 44237-008?
What are the uses for Herbion Naturals Honey-lemon Cough Drops?
Which are Herbion Naturals Honey-lemon Cough Drops UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are Herbion Naturals Honey-lemon Cough Drops Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- EUCALYPTUS OIL (UNII: 2R04ONI662)
- HYSSOPUS OFFICINALIS FLOWERING TOP (UNII: X7HKN4FOJI)
- LESSER GALANGAL ROOT (UNII: 42LD90786Y)
- LICORICE (UNII: 61ZBX54883)
- LONG PEPPER (UNII: 2NMG4EA7B1)
- JUSTICIA ADHATODA LEAF (UNII: HH159XOV81)
- SUCROSE (UNII: C151H8M554)
- VIOLA ODORATA LEAF (UNII: 3X41NMU9FW)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Herbion Naturals Honey-lemon Cough Drops?
- RxCUI: 637116 - menthol 1.6 MG Oral Lozenge
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[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".