NDC 71119-0001 Alcohol Pad

NDC Product Code 71119-0001

NDC CODE: 71119-0001

Proprietary Name: Alcohol Pad 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.

NDC Code Structure

  • 71119 - Suzhou Shunjie Sanitary Materials Co., Ltd.

NDC 71119-0001-1

Package Description: 1 SWAB in 1 POUCH

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

NDC Product Information

Alcohol Pad with NDC 71119-0001 is a product labeled by Suzhou Shunjie Sanitary Materials Co., Ltd.. The product's dosage form is and is administered via form. The RxNorm Crosswalk for this NDC code indicates a single RxCUI concept is associated to this product: 797544.

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: Suzhou Shunjie Sanitary Materials Co., Ltd.
Labeler Code: 71119
Start Marketing Date: 12-27-2016 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 - 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.

Alcohol Pad Product Label Images

Alcohol Pad 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

Alcohol Pad

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Active Ingredient

70% Isopropyl Alcohol




For preparation of the skin prior to injection, infusion, transfusion.

Dosage And Administration

For Swab.For Topical Use.


For external use only.

Do Not Use

● with electrocautery procedures.

● in the eyes, if contact occurs, flush eyes with water.

Stop Use

● if irritation and redness develop;● if condition persists consult your health care practitioner.

Keep Out Of Reach Of Chikdren

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


● Wipe injection, infusion or transfusion site vigorously and discard.

Inactive Ingredient

Purified Water.

* Please review the disclaimer below.