NDC 70242-109 Iodine Tincture White
NDC Product 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.
Non-Proprietary Name: What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
NDC Code Structure
- 70242 - Dannso Corp./d.b.a. Essential Products
- 70242-109 - Iodine Tincture White
NDC 70242-109-01
Package Description: 30 mL in 1 BOTTLE, PLASTIC
NDC Product Information
Iodine Tincture White with NDC 70242-109 is a product labeled by Dannso Corp./d.b.a. Essential Products. The generic name of Iodine Tincture White is . The product's dosage form is and is administered via form.
Labeler Name: Dannso Corp./d.b.a. Essential Products
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.
- 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 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.
Information for Patients
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
- Purpose
- Use
- Warnings
- Inactive Ingredient
- Stop Use And Ask A Doctor
- Keep Out Of Reach Of Children
- Directions
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.
