CLOROX HAND SANITIZER GEL- alcohol hand sanitizer gel

CLOROX Hand sanitizer Gel by

Drug Labeling and Warnings

CLOROX Hand sanitizer Gel by is a Otc medication manufactured, distributed, or labeled by New Wave Global Services Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

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.

Active Ingredient(s)

Alcohol 70% v/v

Purpose

Antiseptic

Use

Hand Sanitizer to help reduce bacteria on the skin.

Warnings

For external use only. Flammable. Keep away from heat or flame

Do not use

• in children less than 2 months of age
• on open skin wounds

WHEN USING

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

STOP USE

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

KEEP OUT OF REACH OF CHILDREN

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

Directions

• Place enough product on hands to cover all surfaces. Rub hands together until dry.
• Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

• Store between 15-30C (59-86F)
• Avoid freezing and excessive heat above 40C (104F)

Inactive ingredients

Water, Acrylates/Vinyl Isodecanoate Crosspolymer (10000 MPA.S Neutralized at 0.5%), Aloe Vera Leaf Extract, Propylene Glycol, Isopropyl Myristate, Fragrance, Vitamin E Acetate, Yellow 10, Yellow 5, Blue 1

Questions?

1-888-325-6769 24 hours, 7 days per week

www.cloroxhandsanitizer.com

Package Label - Principal Display Panel

clorox HS 4OZx12 Carton, NDC: 80714-034-04

CLOROX HS 4OZ Tube, NDC: 80714-034-02

CLOROX HS Gallon Jug- NDC: 80714-034-08

CLOROX HS Pouch-NDC: 80714-034-05

CLOROX HS 24x Single Use Pouches Carton- NDC: 80714-034-06

CLOROX HS 12X2oz Tube Display Carton- NDC: 80714-034-03

CLOROX HS 2OZ Tube-NDC: 80714-034-01

6 x 12 oz Bottles

INGREDIENTS AND APPEARANCE

CLOROX HAND SANITIZER GEL 
alcohol hand sanitizer gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 80714-034
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.7 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
WATER (UNII: 059QF0KO0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
ALOE (UNII: V5VD430YW9)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ACRYLATES/VINYL ISODECANOATE CROSSPOLYMER (10000 MPA.S NEUTRALIZED AT 0.5%) (UNII: 2N8MDB79NA)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 80714-034-03	12 in 1 CARTON	10/30/2020	02/28/2023
1	NDC: 80714-034-01	59 mL in 1 TUBE; Type 0: Not a Combination Product
2	NDC: 80714-034-08	3780 mL in 1 JUG; Type 0: Not a Combination Product	01/20/2021	01/31/2025
3	NDC: 80714-034-06	24 in 1 CARTON	01/20/2021	01/31/2023
3	NDC: 80714-034-05	3 mL in 1 POUCH; Type 0: Not a Combination Product
4	NDC: 80714-034-09	236 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	05/25/2021	02/29/2024
5	NDC: 80714-034-11	6 in 1 CARTON	10/30/2020	03/31/2024
5	NDC: 80714-034-10	354 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
6	NDC: 80714-034-04	12 in 1 CARTON	10/30/2020	03/31/2024
6	NDC: 80714-034-02	118 mL in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	10/30/2020	01/31/2025

Labeler - New Wave Global Services Inc (202806733)