90081-006 74881-006 Hand Sanitizer

Hand Sanitizer by

Drug Labeling and Warnings

Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by FLTR, INC., Huizhou Baozi Biotechnology Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

HAND SANITIZER- hand sanitizer gel 
FLTR, INC.

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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90081-006
74881-006
Hand Sanitizer

Active Ingredient

Ethyl Alcohol 75%

Purpose

Antimicrobial

Uses

Helps reduce bacteria on the s k in

Warnings

Flammable Keep awayfromfireorflame. For external use only.

When using this product do not use in or near the eyes

WHEN USING THIS PRODUCT

When using this product do not use in or near the eyes. Incase of contact, rinese eyes thoroughly with water, Stop use and ask doctor if irritation or rash appears and lasts, Keep out of reach for children. If swallowed , get medical help or contact a Poison Control Center right away.

stop use and ask a doctor if imitation 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

Directions: Place enough product in your palm to thoroughly spread on both hands and rub into the skin until dry

Children under 6 years of age should be supervised when using this product

Other information

Store below 106F(41C).May discolor certain fabnics orsurfaces

Inactive ingredients

nactive Ingredients: water, carbomer, triethanolamine

Package Label - Principal Display Panel

HSC100_Retail box_Hand Sanitizer 4PK

90081-006-01

HAND SANITIZER 
hand sanitizer gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 90081-006
Route of Administration	TOPICAL

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

Inactive Ingredients
Ingredient Name	Strength
CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO)
WATER (UNII: 059QF0KO0R)
TROLAMINE (UNII: 9O3K93S3TK)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 90081-006-01	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/27/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	07/27/2020	01/21/2021

Labeler - FLTR, INC. (117468331)

Registrant - Huizhou Baozi Biotechnology Co., Ltd. (419304583)

Establishment
Name	Address	ID/FEI	Business Operations
FLTR, INC.		117468331	label(90081-006) , manufacture(90081-006)

Revised: 1/2021

Document Id: b96681db-9006-9dc1-e053-2a95a90aa154

34390-5

Set id: ac0a0fb2-ba0d-17ff-e053-2995a90a9343

Version: 3

Effective Time: 20210121

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