HAND SANITIZER SWEET POMEGRANATE- alcohol gel 
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 Sweet Pomegranate

Drug Facts

Active ingredient

Alcohol 66%

Purpose

Antiseptic

Use

  • To decreae bacteria on the skin.

Warnings

  • For external use only.
  • Flammable, keep away from fire & flame
  • Does not contain grain alcohol; do not drink. If taken internally will produce severe gastic disturbances

When using this product

  • Avoid the eyes and mucous membranes
  • In the case of eyes or mucous membrane contact, rinse area thoroughly with water

Stop use and ask a doctor if

  • Condition worsens
  • Redness or irritation develops
  • Condition persists for more than 3 days

Keep out of reach of children.

  • If swallowed contact a doctor or 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

  • Store below 105ºF.
  • May discolor fabrics.

Inactive ingredients:

Water, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, Fragrance, FD&C Red No. 4, D&C Red No.33.

Questions?

Call 1-888-988-2427

Package Labeling:

Label8

HAND SANITIZER SWEET POMEGRANATE 
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62651-067
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL66 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
FD&C RED NO. 4 (UNII: X3W0AM1JLX)  
D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:62651-067-0130 mL in 1 BOTTLE; Type 0: Not a Combination Product09/15/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E09/15/2021
Labeler - BASE4 Ventures, Inc (137316126)
Establishment
NameAddressID/FEIBusiness Operations
Ganzhou Olivee Cosmetic Co., Ltd.543008195manufacture(62651-067)

Revised: 4/2021
 
BASE4 Ventures, Inc