Hand Sanitizer by Dynarex Corporation HAND SANITIZER gel

Hand Sanitizer by

Drug Labeling and Warnings

Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Dynarex Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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 Label

Label

1428 Label

Label

1429 Label

Label

1431 Label

Label

1432 Label

Label

1433 Label

Label

1433UB-10 Label

INGREDIENTS AND APPEARANCE

HAND SANITIZER 
hand sanitizer gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 67777-911
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL 95% (UNII: 7528N5H79B) (ALCOHOL 95% - UNII:7528N5H79B)	ALCOHOL 95%	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
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
Shape	FREEFORM	Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 67777-911-03	6 in 1 CASE	12/05/2025
1	NDC: 67777-911-02	24 in 1 BOX
1	NDC: 67777-911-01	29.5 mL in 1 BOTTLE; Type 0: Not a Combination Product
2	NDC: 67777-911-06	6 in 1 CASE	12/05/2025
2	NDC: 67777-911-05	24 in 1 BOX
2	NDC: 67777-911-04	59 mL in 1 BOTTLE; Type 0: Not a Combination Product
3	NDC: 67777-911-09	4 in 1 CASE	12/05/2025
3	NDC: 67777-911-08	24 in 1 BOX
3	NDC: 67777-911-07	118.3 mL in 1 BOTTLE; Type 0: Not a Combination Product
4	NDC: 67777-911-11	48 in 1 CASE	12/05/2025
4	NDC: 67777-911-10	236.5 mL in 1 BOTTLE; Type 0: Not a Combination Product
5	NDC: 67777-911-13	12 in 1 CASE	12/05/2025
5	NDC: 67777-911-12	473 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
6	NDC: 67777-911-15	12 in 1 CASE	12/05/2025
6	NDC: 67777-911-14	144 in 1 BOX
6		1.01 mL in 1 PACKET; Type 0: Not a Combination Product
7	NDC: 67777-911-17	100 in 1 CASE	12/05/2025
7	NDC: 67777-911-16	10 in 1 BOX
7		1.01 mL in 1 PACKET; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	12/05/2025

Labeler - Dynarex Corporation (008124539)