NDC 37205-989 Alcohol Swab With Benzocaine

NDC Product Code 37205-989

NDC CODE: 37205-989

Proprietary Name: Alcohol Swab With Benzocaine 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

  • 37205 - Cardinal Health

NDC 37205-989-57

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 Swab With Benzocaine with NDC 37205-989 is a product labeled by Cardinal Health. 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: 809206.

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: Cardinal Health
Labeler Code: 37205
Start Marketing Date: 07-01-2007 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 Swab With Benzocaine Product Label Images

Alcohol Swab With Benzocaine 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


Topical AnestheticAntiseptic


  • 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


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.


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)

Inactive Ingredients

Propylene glycol, purified water

Carton Information

NDC 37205-989-57LEADERALCOHOL SWABSWith Benzocaine for PAIN RELIEFAntiseptic / AnestheticIsopropyl Alcohol 70%Safe and easy to use80 SWABS

* Please review the disclaimer below.