NDC 70242-109 Iodine Tincture White

  1. Labeler Index
  2. Dannso Corp./d.b.a. Essential Products
  3. NDC: 70242-109 Iodine Tincture White

NDC Product Code 70242-109

NDC CODE: 70242-109

Proprietary Name: Iodine Tincture White 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.

Drug Use Information

Drug Use Information
The drug use information is a summary and does NOT have all possible information about this product. This information does not assure that this product is safe, effective, or appropriate. This information is not individual medical advice and does not substitute for the advice of a health care professional. Always ask a health care professional for complete information about this product and your specific health needs.
  • This product is used as first aid antiseptic

NDC Code Structure

NDC 70242-109-01

Package Description: 30 mL in 1 BOTTLE, PLASTIC

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

NDC Product Information

Iodine Tincture White with NDC 70242-109 is product labeled by Dannso Corp./d.b.a. Essential Products. The product's dosage form is and is administered via form.

RxNorm Crosswalk

What is RxNorm?
RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) (RxCUI) to each NDC.

The RxNorm Crosswalk for this NDC code indicates a single concept unique identifier (RXCUI) is associated with this product:


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.
  • AMMONIUM SALICYLATE (UNII: 0T3Q181657)
  • ISOPROPYL ALCOHOL (UNII: ND2M416302)
  • SODIUM IODIDE (UNII: F5WR8N145C)
  • WATER (UNII: 059QF0KO0R)

Product Labeler Information

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

Labeler Name: Dannso Corp./d.b.a. Essential Products
Labeler Code: 70242
Start Marketing Date: 08-08-2015 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: 12-31-2017 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.

Information for Patients

Iodine

Iodine is


...
[Read More]

* Please review the disclaimer below.

Iodine Tincture White Product Label Images

Iodine Tincture White 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 Ingredients

Iodine 2%

Purpose

First aid antiseptic

Use

  • First aid to help prevent sking infection inminor cutsscrapesburns

Warnings

WarningsFor external use only. Avoid contact with eyes or with mucous membrane. Keep out of the reach of children. Children under 2 years please consult a physician. Do not apply on irritated skin, in or near eyes or mocuos memebranes, on wounds or damamged skin, or if it causes allergic reaction. In case of accidental ingestion, seek professional assistance or contact Poison Control Center immedialately.

Inactive Ingredient

Ammonium, Deionized Water, Isopropyl Alcohol, Sodium Iodine.

Stop Use And Ask A Doctor

If condition persists or gets worse

Keep Out Of Reach Of Children

If swallowed, get medical help or contact a Poison Control Center right away

Directions

  • Clean the affected area and dry thorougkyapply. Apply a thin layer 1 to 3 times dailyMay be covered with a sterile bandage

* Please review the disclaimer below.