Vaswani Instant Hand Sanitizer: Package Insert and Label Information

VASWANI INSTANT HAND SANITIZER- alcohol gel
Vaswani 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.

Drug Facts

Active Ingredient

Ethyl alcohol 75%

Purpose

Antiseptic

Use

  • for handwashing to decrease bacteria on the hand

Warnings

For external use only.

Flammable. Keep away from fire or flame.

Do not use

  • in the eyes.

Stop use and ask a doctor if

  • irritation and redness develop
  • condition persists for more than 72 hours

Keep out of reach of children.

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

​Directions

  • Wet hands thoroughly with product and allow to dry without wiping.

Other Information

  • Store between 59-86°F (15-30°C)
  • Avoid freezing and excessive heat above 104°F (40°C)

Inactive ingredients

Carbomer, Glycerol, Triethanolamine, Water.

Questions or Comments?

1-800-819-4159

Package Labeling:

Label
(click image for full-size original)

Package Labeling: 3.8L

Bottle
(click image for full-size original)

VASWANI INSTANT HAND SANITIZER
alcohol gel
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:77950-002
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ALCOHOL (ALCOHOL) ALCOHOL 0.75 mL in 1 mL
Inactive Ingredients
Ingredient Name Strength
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE
GLYCERIN
TROLAMINE
WATER
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:77950-002-01 500 mL in 1 BOTTLE None
2 NDC:77950-002-02 3800 mL in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part333E 05/15/2020
Labeler — Vaswani Inc (133132337)

Revised: 05/2020 Vaswani Inc

DrugInserts.com provides trustworthy package insert and label information about marketed drugs as submitted by manufacturers to the US Food and Drug Administration. Package information is not reviewed or updated separately by DrugInserts.com. Every individual package label entry contains a unique identifier which can be used to secure further details directly from the US National Institutes of Health and/or the FDA.

As the leading independent provider of trustworthy medication information, we source our database directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. Our material is not intended as a substitute for direct consultation with a qualified health professional.

Terms of Use | Copyright © 2021. All Rights Reserved.