CLOROX Hand sanitizer Gel by New Wave Global Services Inc

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]

CLOROX HAND SANITIZER GEL- alcohol hand sanitizer gel 
New Wave Global Services Inc

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

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. 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 Hand Sanitizer Gel 12 Oz Bottle-NDC: <a href=/NDC/80714-034-10>80714-034-10</a>

Clorox Hand Sanitizer Gel 8 Oz Bottle-NDC: <a href=/NDC/80714-034-09>80714-034-09</a>

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

CLOROX HS 4OZX12 CARTON

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

Clorox HS 4OZ Tube

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

CLOROX HS Gallon Jug

CLOROX HS Pouch-NDC: 80714-034-05 Clorox HS Pouch- NDC: <a href=/NDC/80714-034-05>80714-034-05</a>

CLOROX HS 24x Single Use Pouches Carton- NDC: 80714-034-06 24x Single Use Pouces Carton NDC: <a href=/NDC/80714-034-06>80714-034-06</a>

CLOROX HS 12X2oz Tube Display Carton- NDC: 80714-034-03 12x2 oz Tubes Display Carton

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

Clorox Hand Sanitizer Gel - 2oz Tube Label NDC: <a href=/NDC/80714-034-01>80714-034-01</a>

6 x 12 oz Bottles

6 x 12 oz Bottles

CLOROX HAND SANITIZER GEL 
alcohol hand sanitizer gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 80714-034
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.7 mL  in 1 mL
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 80714-034-0312 in 1 CARTON10/30/202002/28/2023
1NDC: 80714-034-0159 mL in 1 TUBE; Type 0: Not a Combination Product
2NDC: 80714-034-083780 mL in 1 JUG; Type 0: Not a Combination Product01/20/202101/31/2025
3NDC: 80714-034-0624 in 1 CARTON01/20/202101/31/2023
3NDC: 80714-034-053 mL in 1 POUCH; Type 0: Not a Combination Product
4NDC: 80714-034-09236 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product05/25/202102/29/2024
5NDC: 80714-034-116 in 1 CARTON10/30/202003/31/2024
5NDC: 80714-034-10354 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
6NDC: 80714-034-0412 in 1 CARTON10/30/202003/31/2024
6NDC: 80714-034-02118 mL in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph Drug505G(a)(3)10/30/202001/31/2025
Labeler - New Wave Global Services Inc (202806733)

Revised: 12/2023
Document Id: 0d8507ac-785d-f790-e063-6294a90a2991
Set id: b2e9ab98-d2a6-257b-e053-2a95a90a08f5
Version: 6
Effective Time: 20231227