OTC Medication Information: Hand Sanitizer Eucalyptus Breeze

HAND SANITIZER EUCALYPTUS BREEZE- alcohol spray
BASE4 Ventures, 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

Alcohol Denat. 70% (V/V)

Purpose

Antiseptic

Uses

  • hand sanitizer to help decrease bacteria on the skin.
  • recommended for repeated use.

Warnings

  • For external use only.
  • Flammable.
  • Keep away from heat or flame.
  • Does not contain grain alcohol; do not drink. If taken internally will produce severe gastric disturbances.

When using this product,

do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

Stop use and ask a doctor

if redness or irritation develop and lasts.

Keep out of reach of children.

If swallowed, get medical help or contact a poison control center immediately.

Directions

  • Rub dime sized amount between hands until dry.
  • Supervise children in the use of this product. In the case of eye contact rinse eyes thoroughly with water

Other information

  • Do not store above 105°F.
  • May discolor some fabrics.

Inactive ingredients

D&C Red No.33, Disodium EDTA, FD&C Blue No.1, FD&C Red No.4, FD&C Yellow No.5, Fragrance, Carbomer, Glycerin, Water

Package Labeling:

Back_EB_59
(click image for full-size original)
Bottle_EB_59
(click image for full-size original)
Front_EB_59
(click image for full-size original)
Tube_EB_59
(click image for full-size original)

HAND SANITIZER EUCALYPTUS BREEZE
alcohol spray
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:62651-052
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ALCOHOL (ALCOHOL) ALCOHOL 0.7 mL in 1 mL
Inactive Ingredients
Ingredient Name Strength
D&C RED NO. 33
EDETATE DISODIUM ANHYDROUS
FD&C BLUE NO. 1
FD&C RED NO. 4
FD&C YELLOW NO. 5
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE
GLYCERIN
WATER
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:62651-052-01 59.1 mL in 1 BOTTLE, SPRAY None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part333E 12/04/2020 12/04/2021
Labeler — BASE4 Ventures, Inc (137316126)

Revised: 05/2021 BASE4 Ventures, Inc

Our database comes directly from the FDA’s central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA’s repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

Our database comes directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA's repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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