INSTANT HAND SANITIZER- alcohol gel 
Hydrox Laboratories

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Instant Hand Sanitizer Honey Scent

Drug Facts

Active ingredient

Ethyl Alcohol 70% v/v

Purpose

Antiseptic

Uses

Warnings

Flammable. Keep away from fire or flame

For external use only - hands.

When using this productdo not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

Stop use and ask a physician ifskin irritation or rash develops.

Keep out of reach of children.If accidently ingested, seek medical help or contact a Poison Control Center immediately.

Directions

Other Information

Inactive ingredients

carbomer, fragrance, glycerin, isopropyl alcohol, isopropyl myristate, propylene glycol, purified water, tocopheryl acetate, aloe vera gel, AMP-95

MFG BY: HYDROX LABORATORIES
825 Tollgate Road ELGIN, IL 60123

PRINCIPAL DISPLAY PANEL 

NDC 10565-076-04

Hydrox
Laboratories

INSTANT
HAND
SANITIZER
with moisturizers
aloe & vitamin E

KILLS 99.9%
OF GERMS*

4 FL OZ 118 mL

Made in USA Principal Display Panel - 59 mL Cylinder Label

INSTANT HAND SANITIZER 
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10565-076
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
CARBOMER HOMOPOLYMER TYPE C (UNII: 4Q93RCW27E)  
GLYCERIN (UNII: PDC6A3C0OX)  
ISOPROPYL ALCOHOL (UNII: ND2M416302)  
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
WATER (UNII: 059QF0KO0R)  
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:10565-076-0259 mL in 1 CYLINDER; Type 0: Not a Combination Product01/09/2012
2NDC:10565-076-04118 mL in 1 CYLINDER; Type 0: Not a Combination Product01/09/2012
3NDC:10565-076-08237 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product01/09/2012
4NDC:10565-076-16473 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product01/09/2012
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph Drug505G(a)(3)01/09/2012
Labeler - Hydrox Laboratories (025164302)
Registrant - Hydrox Laboratories (025164302)
Establishment
NameAddressID/FEIBusiness Operations
Hydrox Laboratories025164302manufacture(10565-076) , label(10565-076) , pack(10565-076)

Revised: 10/2023
Document Id: 08a52381-d02b-c869-e063-6294a90a099b
Set id: a818def4-f6e9-4a97-aa26-b7c082ae8d18
Version: 14
Effective Time: 20231026
 
Hydrox Laboratories