NDC 70812-001 White Labs

NDC Product Code 70812-001

NDC 70812-001-02

Package Description: 1 TUBE in 1 CARTON > 15 g in 1 TUBE (70812-001-01)

NDC 70812-001-04

Package Description: 1 PACKAGE in 1 CARTON > 20 g in 1 PACKAGE (70812-001-03)

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

NDC Product Information

White Labs with NDC 70812-001 is a product labeled by Biostech Co., Ltd.. The generic name of White Labs is . The product's dosage form is and is administered via form.

Labeler Name: Biostech Co., Ltd.

Dosage Form: -

Product Type: What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

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.

  • WATER (UNII: 059QF0KO0R)
  • POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990)
  • TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
  • POLOXAMER 407 (UNII: TUF2IVW3M2)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
  • ALCOHOL (UNII: 3K9958V90M)
  • POVIDONE K29/32 (UNII: 390RMW2PEQ)
  • POVIDONE K90 (UNII: RDH86HJV5Z)
  • SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
  • MENTHA SUAVEOLENS WHOLE (UNII: G0O5N5EA8X)
  • CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
  • SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)

Product Labeler Information

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

Labeler Name: Biostech Co., Ltd.
Labeler Code: 70812
Start Marketing Date: 04-01-2018 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: 12-31-2019 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 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. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

White Labs Product Label Images

White Labs 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

Hydrogen Peroxide 2.80%

Otc - Purpose

Oral Debriding

Indications & Usage

Aids in the removal of phlegm, mucus, or other secretions associated with occasional sore mouth

Dosage & Administration

Use up to 2 times daily after meals and at bedtimechildren under 13 years of age Do not use

Warnings

For external use only

Otc - Ask Doctor

The condition persists or gets worseSore mouth symptoms do not improve in 7 daysIrritation, pain or redness persists or worsensSwelling, rash or fever develops

Otc - Keep Out Of Reach Of Children

Keep out of reach of children. If more than used for rinsing is accidentally swallowed, get medical help or contact a Poison Control Center right away

Inactive Ingredient

Distilated water, Polyvinyl alcohol, Titanium dioxide, Poloxamer 407, Glycerine, PEG400, Ethanol, PVP K29/32(Povidone), PVP K90(Povidone), Aerosil 200, Flavor(Applemint HF62184), Citric Acid, Sodium Citric Acid

* Please review the disclaimer below.