NDC 76772-023 Luxury Antiseptic

Hydrogen Peroxide

NDC Product Code 76772-023

NDC 76772-023-17

Package Description: 177 mL in 1 BOTTLE, PLASTIC

NDC Product Information

Luxury Antiseptic with NDC 76772-023 is a a human over the counter drug product labeled by Tsm Ithalat Ihracat Sanayi Ve Dis Ticaret Limited Sirketi. The generic name of Luxury Antiseptic is hydrogen peroxide. The product's dosage form is liquid and is administered via topical form.

Labeler Name: Tsm Ithalat Ihracat Sanayi Ve Dis Ticaret Limited Sirketi

Dosage Form: Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.

Product Type: Human Otc Drug 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.

Luxury Antiseptic Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • HYDROGEN PEROXIDE 30 mg/mL

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)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.

Product Labeler Information

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

Labeler Name: Tsm Ithalat Ihracat Sanayi Ve Dis Ticaret Limited Sirketi
Labeler Code: 76772
FDA Application Number: part333A What is the FDA Application Number?
This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.

Marketing Category: OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final. What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Start Marketing Date: 03-10-2021 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: 12-31-2022 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: N - NO 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.

Luxury Antiseptic Product Label Images

Luxury Antiseptic 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

Active Ingredient

Hydrogen peroxide 3%

Purpose

First aid antiseptic / oral debriding agent

Warnings

For external use only.Ask a doctor before use if you have deep or puncture wounds, animal bites, or serious burns.


Stop use and ask a doctor if *swelling, rash, or fever develops. *the condition persists or gets worse. *sore mouth symptoms do not improve in 7 days. *irritation, pain or redness persists or worsens.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children. If swallowed, get medical help or contact poison control center right away.

Stop Use

Stop use and ask a doctor if *swelling, rash, or fever develops. *the condition persists or gets worse. *sore mouth symptoms do not improve in 7 days. *irritation, pain or redness persists or worsens.

Ask Doctor

Ask a doctor before use if you have deep or puncture wounds, animal bites, or serious burns.

Do Not Use

Do not use *in the eyes or apply over large areas of the body. *longer than one week.

Dosage & Administration

  • Directions For use as a first aid antiseptic: Clean affected area. apply small amount of product on affected area 1-3 times a day.may be covered with a sterile bandage. For use as an oral debriding agent (oral rinse): adults and children 2 years of age and overmix with an equal amount of water.swish around in the mouth over affected area for at least 1 minute and then spit out. Do not swallow. use up to 4 times daily after meals and at bedtime or as directed by a dentist or doctor.children under 12 years should be supervised in the use of this product.
  • Children under 2 years of age: consult a dentist or doctor.

Other Information

  • Keep tightly closed and in a dark place at room temperature. Do not shake bottle. Hold away from face when opening.

Inactive Ingredient

Inactive ingredient purified water

* Please review the disclaimer below.