INSTANT HAND SANITIZER ALOE VERA- ethyl alcohol liquid 
Universal Distribution Center LLC

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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INSTANT HAND SANITIZER ALOE VERA

Active ingredient

Ethyl alcohol  70% v/v

Purpose

Antimicrobial

Use

Warnings

Flammable. Keep away from fire or flame.

For external use only.

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 irritation or rash appears and lasts.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Other information

Inactive ingredients

Water, glycerin, propylene glycol, acrylates/c10-30 alkyl acrylate crosspolymer, isopropyl alcohol, aminomethyl propanol,  isopropyl myristate,  caprylyl glycol, phenoxyethanol, fragrance, tocopheryl acetate, aloe barbadensis gel, FD&C yellow no.5, FD&C blue no.1.

PRINCIPAL DISPLAY PANEL

INSTANT HAND SANITIZER ALOE VERA WITH VITAMIN E AND OTHER MOISTURIZERS

ANTIMICROBIAL

KILLS GERMS WITHOUT WATER

8 FL.OZ (236 mL)

PRINCIPAL DISPLAY PANEL

INSTANT HAND SANITIZER ALOE VERA 
ethyl alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52000-016
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO)  
ISOPROPYL ALCOHOL (UNII: ND2M416302)  
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:52000-016-2959 mL in 1 BOTTLE, PLASTIC
2NDC:52000-016-01118 mL in 1 BOTTLE, PLASTIC
3NDC:52000-016-30236 mL in 1 BOTTLE, PLASTIC
4NDC:52000-016-31295 mL in 1 BOTTLE, PLASTIC
5NDC:52000-016-32354 mL in 1 BOTTLE, PLASTIC
6NDC:52000-016-33472 mL in 1 BOTTLE, PLASTIC
7NDC:52000-016-34708 mL in 1 BOTTLE, PLASTIC
8NDC:52000-016-35944 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E11/22/2014
Labeler - Universal Distribution Center LLC (019180459)

Revised: 12/2014
Document Id: 0929689b-d8e6-5f1e-e054-00144ff8d46c
Set id: 64ed1ec1-69cb-4527-ab71-9ea0bc388a98
Version: 1
Effective Time: 20141226
 
Universal Distribution Center LLC