NDC 49953-2801 Alcohol

NDC Product Code 49953-2801

NDC 49953-2801-1

Package Description: 10 mL in 1 BOX

NDC 49953-2801-2

Package Description: 1 mL in 1 POUCH

NDC 49953-2801-3

Package Description: 3 mL 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 with NDC 49953-2801 is a product labeled by Dalian Rongbang Medical Healthy Devices Co., Ltd.. The generic name of Alcohol is . The product's dosage form is and is administered via form.

Labeler Name: Dalian Rongbang Medical Healthy Devices Co., Ltd.

Alcohol 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.


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: Dalian Rongbang Medical Healthy Devices Co., Ltd.
Labeler Code: 49953
Start Marketing Date: 07-02-2010 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: 12-31-2019 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 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

Dosage & Administration

Two swabsticks saturated with 70% isopropyl alcohol.Apply swabstick to skin.

Inactive Ingredient


Indications & Usage

To clean injection and other catheter sites.Apply swabstick to skin.

Otc - Keep Out Of Reach Of Children


For external use onlyDiscard after single use

Otc - Purpose

Otc - Active Ingredient

Isopropyl alcohol 70 %

* Please review the disclaimer below.