HAND SANITIZER ANTIBACTERIAL WITH MOISTURIZERS AND ALOE 8OZ- alcohol gel
Ningbo Liyuan Daily Chemical Products Co.,Ltd.

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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Active ingredient

Ethyl Alcohol 62.0%

Purpose

Antimicrobial

Uses

hand sanitizer to help reduce bacteria on the skin.

Warnings

For external use only.

Flammable. Keep away from heat and flame.

When using this product

avoid contact with face, eyes, and broken skin. In case of eye contact, flush with plenty of water and seek medical advice.

Stop use and ask a doctor if

irritation or redness develops.

Keep out of reach of children.

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

Directions

wet hands thoroughly with product and rub into skin until dry.
Children under 6 years of age should be supervised by an adult when using this product.

Inactive ingredients

water (aqua), aloe barbadensis (aloe vera) leaf juice, carbomer, fragrance, glycerin, propylene glycol, tocopheryl acetate (vitamin E), triethanolamine, FD&C blue no. 1, FD&C yellow no.5

Drug Facts

label

HAND SANITIZER ANTIBACTERIAL WITH MOISTURIZERS AND ALOE 8OZ
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:76176-061
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
WATER (UNII: 059QF0KO0R)
CARBOMER 934 (UNII: Z135WT9208)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
CUPRIC BIS(TRIETHANOLAMINE) (UNII: YBM44X0B6H)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:76176-061-01	236 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	04/01/2019

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333E	04/01/2019

Labeler - Ningbo Liyuan Daily Chemical Products Co.,Ltd. (530766098)

Registrant - Ningbo Liyuan Daily Chemical Products Co.,Ltd. (530766098)

Name	Address	ID/FEI	Business Operations
Establishment
Ningbo Liyuan Daily Chemical Products Co.,Ltd.		530766098	manufacture(76176-061)