AL-SHIELDS HAND SANITIZER- alcohol gel
YIRONG TRADING (NANJING) 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 75% v/v.

Purpose

Antimicrobial

Use

Hand Sanitizer to help reduce bacteria on the skin that could cause disease.

Warnings

Flammable. Keep away from fire or flame.

For external use only.

When using this product do not use in or near the eyes. In case of contact , rinse eyes thoroughly with water. Avoid using on broken skin.

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

Put enough product in your palm to cover hands and rub hands together until dry.
Children under 6 years of age should be supervised when using this product.

Other Information

Store below 105℉ (40℃).
May discolor certain fabrics.

Inactive ingredients

Water (Aqua), Glycerin, Propylene Glycol, Carbomer, Aminomethyl Propanol, Aloe Barbadensis (Aloe Vera) Gel, Tocopheryl Acetate (Vitamin E)

Package Label - Principal Display Panel

Label

AL-SHIELDS HAND SANITIZER
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:75007-005
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	75 mL in 100 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
CARBOMER HOMOPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: F68VH75CJC)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
.ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:75007-005-01	60 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/01/2020
2	NDC:75007-005-02	236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/01/2020
3	NDC:75007-005-03	300 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/01/2020
4	NDC:75007-005-04	500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/01/2020
5	NDC:75007-005-05	946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/01/2020
6	NDC:75007-005-06	1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/01/2020

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333A	07/01/2020

Labeler - YIRONG TRADING (NANJING) CO., LTD (554529568)