NDC 43347-172 Thera Wise Natural Vapor Rub
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 43347 - Derma Wise Skin Care Ltd.
- 43347-172 - Thera Wise Natural Vapor Rub
Product Characteristics
Product Packages
NDC Code 43347-172-01
Package Description: 1 TUBE in 1 BOX / 28 g in 1 TUBE
Product Details
What is NDC 43347-172?
What are the uses for Thera Wise Natural Vapor Rub?
Which are Thera Wise Natural Vapor Rub UNII Codes?
The UNII codes for the active ingredients in this product are:
- CAMPHOR (NATURAL) (UNII: N20HL7Q941)
- CAMPHOR (NATURAL) (UNII: N20HL7Q941) (Active Moiety)
Which are Thera Wise Natural Vapor Rub 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:
- ARGAN OIL (UNII: 4V59G5UW9X)
- BITTER ORANGE OIL (UNII: 9TLV70SV6I)
- CASTOR OIL (UNII: D5340Y2I9G)
- EUCALYPTUS OIL (UNII: 2R04ONI662)
- HYDROGENATED OLIVE OIL (UNII: 53839415GI)
- OLIVE OIL (UNII: 6UYK2W1W1E)
- OLEA EUROPAEA (OLIVE) OIL UNSAPONIFIABLES (UNII: XO45V955LT)
- SQUALANE (UNII: GW89575KF9)
- MENTHA PIPERITA LEAF (UNII: A389O33LX6)
- PINE NEEDLE OIL (PINUS SYLVESTRIS) (UNII: 5EXL5H740Y)
- TOXICODENDRON VERNICIFLUUM FRUIT RIND WAX (UNII: 6RG2461FCH)
- ROSA MOSCHATA OIL (UNII: J99W255AWF)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- THYME OIL (UNII: 2UK410MY6B)
What is the NDC to RxNorm Crosswalk for Thera Wise Natural Vapor Rub?
- RxCUI: 1806673 - camphor 4.8 % Topical Ointment
- RxCUI: 1806673 - camphor 0.048 MG/MG 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".