CLOROX HAND SANITIZER- alcohol gel Brand Buzz LLCDisclaimer: Most OTC drugs are not reviewed and approved by FDA, however they maybe marketed if they comply with applicable regulations and policies. FDA has notevaluated whether this product complies.

----------Clorox Hand Sanitizer

Drug Facts

Active ingredientEthyl Alcohol 71% v/v

PurposeAntiseptic

UseHand sanitizer to help reduce bacteria on the skin. Recommended for repeated use.

WarningsFor external use only. Flammable. Keep away from fire or flame.

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

Discontinue useif irritation and redness develop. If condition persists for more than 72 hours consult aphysician.

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

DirectionsSqueeze gel into your palm and briskly rub hands together until dry.Children under 6 years of age should be supervised when in use.

Other informationStore between 15 and 30C (59 and 86F).Avoid freezing and excessive heat above 40C (104F).

Inactive ingredientsAloe Barbadensis Leaf Extract, Carbomer, Glycerin, Tocopheryl Acetate (Vitamin E),Triethanolamine, Water (Aqua).

Package Labeling:2ml

Package Labeling:500ml

Package Labeling:1000ml

Package Labeling:1000ml Refill

CLOROX HAND SANITIZER alcohol gel

Product InformationProduct Type HUMAN OTC DRUG Item Code (Source) NDC:69540-0025

Route of Administration TOPICAL

Active Ingredient/Active MoietyIngredient Name Basis of Strength Strength

ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 71 mL in 100 mL

Inactive IngredientsIngredient Name Strength

ALOE VERA LEAF (UNII: ZY81Z83H0X)

Brand Buzz LLC

CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC) GLYCERIN (UNII: PDC6A3C0OX) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) TROLAMINE (UNII: 9O3K93S3TK) WATER (UNII: 059QF0KO0R)

Packaging# Item Code Package Description Marketing Start

DateMarketing End

Date1 NDC:69540-

0025-1 100 in 1 BOX 03/19/2021

1 2 mL in 1 PACKET; Type 0: Not a CombinationProduct

2 NDC:69540-0025-2

500 mL in 1 BOTTLE; Type 0: Not a CombinationProduct 03/19/2021

3 NDC:69540-0025-3

1000 mL in 1 BOTTLE; Type 0: Not a CombinationProduct 03/19/2021

4 NDC:69540-0025-4

1000 mL in 1 BOTTLE; Type 0: Not a CombinationProduct 03/19/2021

Marketing InformationMarketingCategory

Application Number or MonographCitation

Marketing StartDate

Marketing EndDate

OTC monograph notfinal part333E 03/19/2021

Labeler - Brand Buzz LLC (079266204)

Revised: 3/2021