Hand Sanitizer Spray Eucalyptus Breeze

Hand Sanitizer Eucalyptus Breeze by

Drug Labeling and Warnings

Hand Sanitizer Eucalyptus Breeze by is a Otc medication manufactured, distributed, or labeled by BASE4 Ventures, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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.

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Hand Sanitizer Spray Eucalyptus Breeze

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_59Bottle_EB_59Front_EB_59Tube_EB_59

HAND SANITIZER EUCALYPTUS BREEZE 
alcohol spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 62651-052
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.7 mL  in 1 mL
Inactive Ingredients
Ingredient NameStrength
D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
FD&C RED NO. 4 (UNII: X3W0AM1JLX)  
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
GLYCERIN (UNII: PDC6A3C0OX)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 62651-052-0159.1 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product12/04/202012/04/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E12/04/202012/04/2021
Labeler - BASE4 Ventures, Inc (137316126)

Revised: 5/2021
 

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