NDC 55315-809 Alcohol

NDC Product Code 55315-809

NDC 55315-809-30

Package Description: 100 PACKET in 1 BOX > 1 APPLICATOR in 1 PACKET > 5 mL in 1 APPLICATOR

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

NDC Product Information

Alcohol with NDC 55315-809 is a product labeled by Fred's Inc.. 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: Fred's Inc.
Labeler Code: 55315
Start Marketing Date: 04-05-2011 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

Active Ingredient

Isopropyl alcohol, 70% v/v




  • For preparation of the skin prior to injection


For external use only.

When Using This Product

  • Do not get into eyesapply over large areas of the body. In case of deep or puncture wounds, animal bites or serious burns, consult a doctor.

Stop Use And Ask A Doctor If

  • Condition persists or gets worse or lasts for more than 72 hoursdo not use longer than 1 week unless directed by a doctor


  • Keep away from fire or flameDo not use with electrocautery proceduresUse only in a well-ventilated area, fumes may be toxic

Keep Out Of Reach Of Children.

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


Wipe injection site vigorously. Discard after single use.

Other Information

Protect from freezing and avoid excessive heat.

Inactive Ingredients


Package/Label Back

Fred's Alcohol Swabs Box Top, Back, Side, Bottom

* Please review the disclaimer below.