NDC 61767-305 Alcohol

Product Information

Product Packages

NDC 61767-305-01

Package Description: 473 mL in 1 BOTTLE

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

Product Details

Alcohol is product labeled by Blossom Pharmaceuticals. The product's dosage form is and is administered via form.


What are Alcohol Active Ingredients?

The following is the list of active ingredients in this product. An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

  • ISOPROPYL ALCOHOL (UNII: ND2M416302)
  • ISOPROPYL ALCOHOL (UNII: ND2M416302) (Active Moiety)


NDC to RxNorm Crosswalk

What is RxNorm? RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct code indicates a single concept unique identifier (RXCUI) is associated with this product:


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)


* Please review the disclaimer below.

Alcohol Labeling and Warnings

FDA filings in the form of structured product labels are documents that include all published material associated whith this product. Product label information includes data like indications and usage generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Table of Contents



Otc - Active Ingredient



Active Ingredient                                       Purpose

Isopropyl Alcohol 99% v/v                         Antiseptic


Purpose



First aid to help prevent the risk of infection in:

  • minor cuts
  • scrapes
  • burns

Warnings



  • For external use only
  • Flammable, keep away from fire or flame, heat, spark, electrical.
  • Not for use with electrocautinary devices or procedures
  • Ask a doctor before use if you have deep puncture wounds, animal bites or serious burns.
  • Stop use and ask a doctor if condition persist or gets worse.
  • For rubbing and massaging:

    • Caution: Do not apply to irritated skinor if excessive irritation develops
    • Avoid getting into eyes or mucous membranes

Indications & Usage



When using this product:

  • do not get in eyes
  • do not apply over large areas of the body
  • do not use longer than 1 week unless directed by a doctor

Keep Out Of Reach Of Children



Keep out of reach of children.

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


Dosage & Administration



DIRECTIONS:

  • clean the affected area
  • apply a small amount of this product on the affected area 1 to 3 times daily
  • may be covered with a sterile bandage
  • if bandaged let dry first

Other Information



  • Store at room temperature: 15 deg C to 30 deg C   59 deg F to 86 deg F
  • avoid excessive heat
  • Does not contain, nor is it intended as a substitute for grain or ethyl alcohol
  • Will produce serious gastric disturbances if taken internally

Inactive Ingredient



Inactive Ingredient

  • Water

Principal Display Panel



DYNAREX 99% ISOPROPYL ALCOHOL

99 IPA BP.jpg


* Please review the disclaimer below.