HAND SANITIZER- hand sanitizer gel 
Dynarex Corporation

----------

1427 Hand Sanitizer
1428 Hand Sanitizer
1429 Hand Sanitizer
1431 Hand Sanitizer
1432 Hand Sanitizer
1433 Hand Sanitizer
1433UB-10 Hand Sanitizer

Active ingredient

Alcohol 70% V/V

Purpose

Antiseptic Handwash

Use

For hand washing to decrease bacteria on the skin

Warnings

For external use only

Flammable: Keep away from fire or flame

When using this product

• Do not get in the eyes

Stop use and ask a doctor if

irritation and redness develop

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Directions

Wet hands thoroughly with product and allow to dry without wiping

Other information

• Store at room temperature (15º - 30ºC) (59º - 86ºF)

• Recommended for repeated use

Inactive ingredients

acrylates/C10-30 alkyl acrylate crosspolymer (60000 MPA.S), aloe barbadensis leaf juice, aminomethyl propanol, denatonium benzoate, fragrance, glycerin, propylene glycol, tocopheryl acetate, water

Label

1427_BX_MASTER1427 Label

Label

1428_BX_MASTER1428 Label

Label

1429_BX_MASTER1429 Label

Label

1431_IN_MASTER1431 Label

Label

1432_IN_MASTER1432 Label

Label

1433_BX_MASTER1433 Label

Label

1433UB-10_BX_MASTER1433UB-10 Label

HAND SANITIZER 
hand sanitizer gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67777-911
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL 95% (UNII: 7528N5H79B) (ALCOHOL 95% - UNII:7528N5H79B) ALCOHOL 95%70 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
ALOE BARBADENSIS LEAF (UNII: ZY81Z83H0X)  
DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)  
ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S) (UNII: 8Z5ZAL5H3V)  
AMINOMETHYL PROPANOL (UNII: LU49E6626Q)  
GLYCERIN (UNII: PDC6A3C0OX)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
Product Characteristics
Color    Score    
ShapeFREEFORMSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:67777-911-036 in 1 CASE12/05/2025
1NDC:67777-911-0224 in 1 BOX
1NDC:67777-911-0129.5 mL in 1 BOTTLE; Type 0: Not a Combination Product
2NDC:67777-911-066 in 1 CASE12/05/2025
2NDC:67777-911-0524 in 1 BOX
2NDC:67777-911-0459 mL in 1 BOTTLE; Type 0: Not a Combination Product
3NDC:67777-911-094 in 1 CASE12/05/2025
3NDC:67777-911-0824 in 1 BOX
3NDC:67777-911-07118.3 mL in 1 BOTTLE; Type 0: Not a Combination Product
4NDC:67777-911-1148 in 1 CASE12/05/2025
4NDC:67777-911-10236.5 mL in 1 BOTTLE; Type 0: Not a Combination Product
5NDC:67777-911-1312 in 1 CASE12/05/2025
5NDC:67777-911-12473 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
6NDC:67777-911-1512 in 1 CASE12/05/2025
6NDC:67777-911-14144 in 1 BOX
61.01 mL in 1 PACKET; Type 0: Not a Combination Product
7NDC:67777-911-17100 in 1 CASE12/05/2025
7NDC:67777-911-1610 in 1 BOX
71.01 mL in 1 PACKET; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00312/05/2025
Labeler - Dynarex Corporation (008124539)

Revised: 12/2025
Document Id: 450e56f0-b8af-072a-e063-6394a90a2d4b
Set id: 450e56f0-b8ae-072a-e063-6394a90a2d4b
Version: 1
Effective Time: 20251203
 
Dynarex Corporation