NDC 10157-9860 Blistex Cold And Allergy Lip Soother
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 10157 - Blistex Inc
- 10157-9860 - Blistex
Product Packages
NDC Code 10157-9860-1
Package Description: 1 CYLINDER in 1 CARTON / 4.25 g in 1 CYLINDER
Product Details
What is NDC 10157-9860?
What are the uses for Blistex Cold And Allergy Lip Soother?
Which are Blistex Cold And Allergy Lip Soother UNII Codes?
The UNII codes for the active ingredients in this product are:
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DIMETHICONE (UNII: 92RU3N3Y1O) (Active Moiety)
- PRAMOXINE HYDROCHLORIDE (UNII: 88AYB867L5)
- PRAMOXINE (UNII: 068X84E056) (Active Moiety)
Which are Blistex Cold And Allergy Lip Soother 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:
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- CHAMOMILE (UNII: FGL3685T2X)
- ETHYL MENTHANE CARBOXAMIDE (UNII: 6S7S02945H)
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- HONEY (UNII: Y9H1V576FH)
- LANOLIN (UNII: 7EV65EAW6H)
- MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)
- MYRISTYL MYRISTATE (UNII: 4042ZC00DY)
- PARAFFIN (UNII: I9O0E3H2ZE)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- WATER (UNII: 059QF0KO0R)
- EUROPEAN ELDERBERRY (UNII: BQY1UBX046)
- SODIUM ASCORBYL PHOSPHATE (UNII: 836SJG51DR)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
- TRIDECYL NEOPENTANOATE (UNII: 3Z8H1DA7J5)
- TANGERINE (UNII: KH3E3096OO)
- CERESIN (UNII: Q1LS2UJO3A)
- TROLAMINE (UNII: 9O3K93S3TK)
What is the NDC to RxNorm Crosswalk for Blistex Cold And Allergy Lip Soother?
- RxCUI: 1234339 - dimethicone 2 % / pramoxine HCl 1 % Topical Ointment
- RxCUI: 1234339 - dimethicone 0.02 MG/MG / pramoxine hydrochloride 0.01 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".