70%: Package Insert and Label Information

70%- isopropyl alcohol liquid
Geiss, Destin & Dunn, Inc

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Active ingredient

Isopropyl alcohol 70%


First Aid Antiseptic


First aid to help prevent the risk of infection in:

  • minor cuts
  • scrapes
  • burns


For external use only


Keep away from fire or flame, heat, spark, electrical

Ask a Doctor before use

for deep or puncture wounds, animal bites or serious burns

When using theis product

  • do not get into eyes
  • do not inhale
  • do not apply over large areas of the body
  • do not use longer than 1 week

Stop use and ask a doctor

If condition persists or gets worse

Keep out of reach of children

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


Fumes can be acutely irritating to skin, eyes and the respiratory system. Do not apply to irritated skin or if excessive irritation develops. Avoid getting into the eyes or on mucous membranes. Avoid inhaling this product.


  • clean the affected area
  • spray 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

  • does not contain, nor is intended as a substitute for grain or ethyl alcohol
  • will produce serious gastric disturbances if taken internally

Inactive ingredients


Distributed By: Geiss, Destin & Dunn, Inc

Peachtree City, GA 30269


principal display panel

NDC 50804-810-72


70% Isopropyl Alcohol

  • First Aid Antisetpic

WARNING FLAMMABLE Keep away from heat, spark, electrical, fire or flame

Use only in a well-ventilated area; fumes can be harmful

CAUTION: Do not point at self or others; product will squirt when squeezed

10 FL OZ (295 mL)

image description
(click image for full-size original)
isopropyl alcohol liquid
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:50804-810
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Inactive Ingredients
Ingredient Name Strength
# Item Code Package Description Multilevel Packaging
1 NDC:50804-810-43 473 mL in 1 BOTTLE, PLASTIC None
2 NDC:50804-810-45 946 mL in 1 BOTTLE, PLASTIC None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part333A 04/08/2010
Labeler — Geiss, Destin & Dunn, Inc (076059836)
Registrant — Vi-Jon, LLC (790752542)
Name Address ID/FEI Operations
Vi-Jon, LLC 790752542 manufacture (50804-810)

Revised: 06/2021 Geiss, Destin & Dunn, Inc

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