GRAPE FRUIT HAND SANITIZER- ethyl alcohol gel

Grape Fruit Hand Sanitizer by

Drug Labeling and Warnings

Grape Fruit Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by SHANDISHI Biological Technology Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DRUG FACTS

Active ingredient

Ethyl Alcohol 70% v/v

Purpose

Antiseptic

Uses

For Hand Sanitizing

Warnings

Warnings: For external use only-hands.
Flammable: Keep away from heat and flame.
When using this product Keep out of eyes. In case of
contact with eyes, flush thoroughly with water.●Avoid contact with
broken skin.●Do not inhale or ingest.
Stop use and ask a doctor
if skin irritation develops.

Keep out of reach of children.

Keep out of reach of children

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

Directions

Wet hands thoroughly with product and allow to
dry without wiping●For children under 6 use only under adult
Supervision.●Not recommended for infants.

Other information

Do not store above 105°F
May discolor some fabrics

Hamful to wood finishes and plastics.

Inactive ingredients

Aloe Vera Leaf Juice,Grapefruit Oil, Glycerin,Triethanolamine,Carbomer,Water.

Package Labeling

INGREDIENTS AND APPEARANCE

GRAPE FRUIT HAND SANITIZER 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 77753-005
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
VITIS VINIFERA FRUIT OIL (UNII: YQ5Q4Y2Z8U)
GLYCERIN (UNII: PDC6A3C0OX)
TROLAMINE (UNII: 9O3K93S3TK)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 77753-005-01	12 in 1 BOX	07/15/2020
1		30 mL in 1 BOTTLE; Type 0: Not a Combination Product
2	NDC: 77753-005-02	12 in 1 BOX	07/15/2020
2		53 mL in 1 BOTTLE; Type 0: Not a Combination Product
3	NDC: 77753-005-03	12 in 1 BOX	07/15/2020
3		60 mL in 1 BOTTLE; Type 0: Not a Combination Product
4	NDC: 77753-005-04	2 in 1 BOX	07/15/2020
4		250 mL in 1 BOTTLE; Type 0: Not a Combination Product
5	NDC: 77753-005-05	12 in 1 BAG	07/15/2020
5		300 mL in 1 BOTTLE; Type 0: Not a Combination Product
6	NDC: 77753-005-06	8 in 1 BOX	07/15/2020
6		350 mL in 1 BOTTLE; Type 0: Not a Combination Product
7	NDC: 77753-005-07	8 in 1 BOX	07/15/2020
7		400 mL in 1 BOTTLE; Type 0: Not a Combination Product
8	NDC: 77753-005-08	8 in 1 BOX	07/15/2020
8		500 mL in 1 BOTTLE; Type 0: Not a Combination Product
9	NDC: 77753-005-09	4 in 1 BOX	07/15/2020
9		750 mL in 1 BOTTLE; Type 0: Not a Combination Product
10	NDC: 77753-005-10	4 in 1 BOX	07/15/2020
10		1000 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	07/15/2020

Labeler - SHANDISHI Biological Technology Co., Ltd. (411868994)

Establishment
Name	Address	ID/FEI	Business Operations
SHANDISHI Biological Technology Co., Ltd.		411868994	manufacture(77753-005)