SNP MY FIRST HAND SANITIZER- alcohol gel

SNP MY FIRST HAND SANITIZER by

Drug Labeling and Warnings

SNP MY FIRST HAND SANITIZER by is a Otc medication manufactured, distributed, or labeled by SD BIOTECHNOLOGIES CO., LTD, Natuzen Co.,Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredients: Ethanol 70%

PURPOSE

Purpose: Hand Sanitizer

WARNINGS

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.
Stop use and ask a doctor if irritation or rash appears
and lasts.
Keep out of reach of children and pets.
Do not eat.
If swallowed, get medical help or contact a Poison Control Center right away.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

Uses

Uses:
Hand sanitizer to help reduce germs on the skin

Directions

Directions:
Apply a dime sized amount of hand sanitizer to the palm of one hand. Rub hands together covering all surfaces of hands and fingers until dry.
Children under 6 years of age should be supervised when using. Not recommended for infants.

INACTIVE INGREDIENT

Inactive ingredients:

Glycyrrhiza Extract, Green Tea Extract, Rosemary Extract, Butylene Glycol, Aloe Extract(09), Water, Carbomer, Triethanolamine

PACKAGE LABEL - SNP MY FIRST HAND SANITIZER 500mL

PACKAGE LABEL - SNP MY FIRST HAND SANITIZER 60mL

INGREDIENTS AND APPEARANCE

SNP MY FIRST HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70142-112
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	350 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
LICORICE (UNII: 61ZBX54883)
GREEN TEA LEAF (UNII: W2ZU1RY8B0)
Butylene Glycol (UNII: 3XUS85K0RA)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
TROLAMINE (UNII: 9O3K93S3TK)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70142-112-01	500 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	03/01/2020
2	NDC: 70142-112-02	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	03/01/2020

Labeler - SD BIOTECHNOLOGIES CO., LTD (688278067)

Registrant - SD BIOTECHNOLOGIES CO., LTD (688278067)

Establishment
Name	Address	ID/FEI	Business Operations
Natuzen Co.,Ltd.		688201272	manufacture(70142-112)