PERSONAL CARE HAND SANITIZER WITH MOISTURIZERS VITAMIN E- ethyl alcohol liquid
Delta Brands & Products LLC

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.

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Drug Facts

Active ingredient

Ethyl Alcohol 62% v/v

Purpose

Antimicrobial

Use

hand sanitizer to help reduce bacteria on the skin

Warnings

Flammable. Keep away from fire and flame. For external use only

When using this product

■ do not use i or near the eyes. In case of contact, rinse eyes thoroughly with water.

Stop use and ask a doctor if

■irritation or rash appears and lasts

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

■ place enough product in your palm to thoroughly spread on both hands and rub into the skin until dry ■ children under 6 years of age should be supervised when using this product

Other infromation

■ store below 105ºF(41ºC) ■ may discolor certain fabrics or surfaces

Inactive ingredients

water, aloe barbadensis leaf juice,carbomer, fragrance, glycerin, propylene glycol, tocopheryl acetate (vitamin E), triethanolamine

Package Label

PERSONAL CARE HAND SANITIZER WITH MOISTURIZERS VITAMIN E
ethyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:72133-051
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	62 mL in 100 mL

Ingredient Name	Strength
Inactive Ingredients
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
ALPHA-TOCOPHEROL (UNII: H4N855PNZ1)
TROLAMINE (UNII: 9O3K93S3TK)
WATER (UNII: 059QF0KO0R)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:72133-051-08	236 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	04/05/2018
2	NDC:72133-051-12	355 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	04/05/2018
3	NDC:72133-051-02	50 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	04/05/2018

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333A	04/05/2018

Labeler - Delta Brands & Products LLC (080999173)