NDC 70781-002 Blanx White Shock
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 70781 - Coswell Spa
- 70781-002 - Blanx White Shock
Product Characteristics
Product Packages
NDC Code 70781-002-01
Package Description: 75 g in 1 TUBE
Product Details
What is NDC 70781-002?
What are the uses for Blanx White Shock?
Which are Blanx White Shock UNII Codes?
The UNII codes for the active ingredients in this product are:
- SODIUM MONOFLUOROPHOSPHATE (UNII: C810JCZ56Q)
- FLUORIDE ION (UNII: Q80VPU408O) (Active Moiety)
Which are Blanx White Shock 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:
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- SILICA DIMETHYL SILYLATE (UNII: EU2PSP0G0W)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
- PVP/VA COPOLYMER (UNII: D9C330MD8B)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
- GLYCERIN (UNII: PDC6A3C0OX)
- CETRARIA ISLANDICA SUBSP. ISLANDICA (UNII: BJ7YPN79A1)
- TRIBASIC CALCIUM PHOSPHATE (UNII: 91D9GV0Z28)
- WATER (UNII: 059QF0KO0R)
- SORBITOL (UNII: 506T60A25R)
- HYDRATED SILICA (UNII: Y6O7T4G8P9)
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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".