NDC 70718-001 Alcohol Swab

  1. Labeler Index
  2. Yantai Daimyung Babycare Supplies Co.,ltd.
  3. NDC: 70718-001 Alcohol Swab

NDC Product Code 70718-001

NDC CODE: 70718-001

Proprietary Name: Alcohol Swab 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

NDC 70718-001-01

Package Description: 400 BOX in 1 BOX > 200 SWAB in 1 BOX

NDC 70718-001-02

Package Description: 300 BAG in 1 BOX > 25 SWAB in 1 BAG

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

NDC Product Information

Alcohol Swab with NDC 70718-001 is a product labeled by Yantai Daimyung Babycare Supplies Co.,ltd.. The generic name of Alcohol Swab is . The product's dosage form is and is administered via form.

Labeler Name: Yantai Daimyung Babycare Supplies 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)

Product Labeler Information

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

Labeler Name: Yantai Daimyung Babycare Supplies Co.,ltd.
Labeler Code: 70718
Start Marketing Date: 08-18-2016 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: 12-31-2017 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.

Alcohol Swab Product Label Images

Alcohol Swab 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

Isopropyl Alcohol 70%v/v

Purpose

Antiseptic

Use

For preparation of skin prior to injection.

Warnings

For External use only.Flammable,keep away from fire or flame.Do not use with electrocautery procedures in eyes.Stop use and ask a doctor if irritation and redness develop,condition persists for more than 72 hours .

Keep Out Of Reach Of Children

In case of accidental ingestion, seek professional assistance or consult a PoisonControl Center immediately.

Directions

Wipe injection site vigorously and discard.

Inactive Ingredients

Purified water

* Please review the disclaimer below.