SNP MY FIRST HAND SANITIZER: Package Insert and Label Information

SNP MY FIRST HAND SANITIZER- alcohol gel
SD BIOTECHNOLOGIES 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.

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

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PACKAGE LABEL — SNP MY FIRST HAND SANITIZER 60mL

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SNP MY FIRST HAND SANITIZER
alcohol gel
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:70142-112
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ALCOHOL (ALCOHOL) ALCOHOL 350 g in 100 mL
Inactive Ingredients
Ingredient Name Strength
Water
LICORICE
GREEN TEA LEAF
Butylene Glycol
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE
TROLAMINE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:70142-112-01 500 mL in 1 BOTTLE, PUMP None
2 NDC:70142-112-02 60 mL in 1 BOTTLE None
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 Operations
Natuzen Co.,Ltd. 688201272 manufacture (70142-112)

Revised: 04/2020 SD BIOTECHNOLOGIES CO., LTD

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