NDC 75978-3048 Thai Herbal Balm Lemon Grass
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 75978 - Thai Herb And Spa
- 75978-3048 - Thai Herbal Balm Lemon Grass
Product Characteristics
Product Packages
NDC Code 75978-3048-1
Package Description: 1 JAR in 1 BOX / 50 g in 1 JAR
NDC Code 75978-3048-2
Package Description: 1 JAR in 1 BOTTLE / 20 g in 1 JAR
Product Details
What is NDC 75978-3048?
What are the uses for Thai Herbal Balm Lemon Grass?
Which are Thai Herbal Balm Lemon Grass UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
- METHYL SALICYLATE (UNII: LAV5U5022Y)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
Which are Thai Herbal Balm Lemon Grass 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:
- WEST INDIAN LEMONGRASS OIL (UNII: 5BIA40E9ED)
- PEPPERMINT OIL (UNII: AV092KU4JH)
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
- PARAFFIN (UNII: I9O0E3H2ZE)
- PETROLATUM (UNII: 4T6H12BN9U)
What is the NDC to RxNorm Crosswalk for Thai Herbal Balm Lemon Grass?
- RxCUI: 1362693 - menthol 10 % / methyl salicylate 12 % Topical Ointment
- RxCUI: 1362693 - menthol 0.1 MG/MG / methyl salicylate 0.12 MG/MG Topical Ointment
- RxCUI: 1362693 - menthol 5 GM / methyl salicylate 6 GM per 50 GM Topical Ointment
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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".