NDC 70781-002 Blanx White Shock

NDC Product Code 70781-002

NDC CODE: 70781-002

Proprietary Name: Blanx White Shock What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Product Characteristics

Color(s):
BLUE (C48333 - CI 42090)

NDC Code Structure

  • 70781 - Coswell Spa

NDC 70781-002-01

Package Description: 75 g in 1 TUBE

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Blanx White Shock with NDC 70781-002 is a product labeled by Coswell Spa. The product's dosage form is and is administered via form.

Inactive Ingredient(s)

About the Inactive Ingredient(s)
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.

  • 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)

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Coswell Spa
Labeler Code: 70781
Start Marketing Date: 06-14-2016 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2020 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.

Exclude Flag: I - INACTIVATED, the listing data was inactivated by the FDA. 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".

* Please review the disclaimer below.

Blanx White Shock Product Label Images

Blanx White Shock Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Otc - Active Ingredient

ACTIVE INGREDIENTSODIUM MONOFLUOROPHOSPHATE

Inactive Ingredient

INACTIVE INGREDIENTSCETRARIA ISLANDICA EXTRACTAQUAHYDROXYPATITESORBITOLHYDRATED SILICAGLYCERINSILICAISOPROPYL ALCOHOLSODIUM LAURYL SULFATECELLULOSE GUMAROMACI 77891SODIUM SACCHARINPVM/MA COPOLYMERSODIUM BENZOATEBENZYL ALCOHOLPHENOXYETHANOLCI 42090

Otc - Purpose

Naturally whitens and removes

bacteria that cause plaque and tooth decay

Otc - Keep Out Of Reach Of Children

Keep out of reach of children

Dosage & Administration

For best results use twice a day

Indications & Usage

For best results apply twice a day

Warnings

WARNING..DO NOT SWALLOW

* Please review the disclaimer below.