NDC 11673-141 Alcohol Prep Pads

NDC Product Code 11673-141

NDC 11673-141-31

Package Description: 80 PACKET in 1 CARTON > 1 SWAB in 1 PACKET

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

NDC Product Information

Alcohol Prep Pads with NDC 11673-141 is a product labeled by Target Corporation. The generic name of Alcohol Prep Pads is . The product's dosage form is and is administered via form.

Labeler Name: Target Corporation

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.

  • PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
  • 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: Target Corporation
Labeler Code: 11673
Start Marketing Date: 02-19-2010 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: 12-31-2017 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 Prep Pads Product Label Images

Alcohol Prep Pads 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

Benzocaine 6%Isopropyl alcohol 70% v/v

Purpose

Topical AnestheticAntiseptic

Uses

  • For preparation of the skin prior to injectionFor temporary relief of pain and itching associated with minor burns, sunburn, minor skin irritations, or insect bites

Warnings

For external use only. Flammable, keep away from fire or flame.

Do Not Use

  • In the eyeswith electrocautery procedures

Stop Use And Ask A Doctor

  • If irritation and redness developif symptoms persist for more than 72 hours or symptoms clear up and occur within a few days.

Ask A Doctor Or Pharmacist

If you are pregnant or nursing a baby.

Keep Out Of Reach Of Children

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

Directions

Prior to Injection - Adults and children 2 years of age or older:Apply to the skin just prior to injection. Benzocaine takes a minute to act. for best results, wait briefly and then make injection.Insect bites, skin irritations, minor burns, sunburn - Adults and children 2 years of age or older:Apply to the affected site not more than 3 to 4 times daily.Children under 2 years of age: Ask a doctor.

Other Information

  • Store at room temperature: 15° - 30° C (59° - 86° F)Do not use to clean and disinfect medical devices or on hard surfaces

Inactive Ingredients

Propylene glycol, water

Questions?

Call 1-800-910-6874

Package Information

NDC 11673-141-31alcohol prep pads with benzocaineantiseptic/anestheticfor preparation of the skinprior to injectionup and up80 count80 INDIVIDUALLY WRAPPED PADS245 10 0155 ID120478Distributed by Target CorporationMinneapolis, MN 55403Made in U.S.A©2010 Target Brands, Inc. All Rights Reserved. Shop Target.com

* Please review the disclaimer below.