DISINFECTION WASH FREE HAND SANITIZER- sodium hypochlorite liquid

Disinfection Wash Free Hand Sanitizer by

Drug Labeling and Warnings

Disinfection Wash Free Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Davemed Healthcare Co., Ltd., Davemed Healthcare Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredient

Sodium hypochlorite

PURPOSE

Purpose

Antiseptic

INDICATIONS & USAGE

Uses

Hand sanitizer to help reduce bacteria on the skin recommended for repeated use.

WARNINGS

Warnings

• Flammable
• Keep away from fire or flame
• For external use only

When using this product

• avoid contact with eyes in case of eye contact immediately flush eyes with water, call a doctor
• avoid contact with broken skin
• Discontinue use if irritation or redness develops. If condition persists from more than 72 hours, consult a doctor

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. Children should only use this product unde adult supervision. Do not drink. Not edible. In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

OTHER SAFETY INFORMATION

Other information

• Do not store above 150F.
• May discolor some fabrics
• Harmful to wood finishes and plastics

DOSAGE & ADMINISTRATION

Directions

• Place enough product in your palm to thoroughly spread on both hands and rub into the skin until dry. Recommended for repeated use.

INACTIVE INGREDIENT

Inactive ingredients

aloe barbadensis leaf extract, caprylyl glycol, carbomer, glycerin siopropyl alcohol, isopropyl alcohol myristate, Hyrochloric acid, sodium chloride

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DISINFECTION WASH FREE HAND SANITIZER 
sodium hypochlorite liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70897-010
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM HYPOCHLORITE (UNII: DY38VHM5OD) (HYPOCHLORITE ION - UNII:T5UM7HB19N)	SODIUM HYPOCHLORITE	120 mg  in 1000 mL

Inactive Ingredients
Ingredient Name	Strength
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
GLYCERIN (UNII: PDC6A3C0OX)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70897-010-01	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/02/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		04/02/2020

Labeler - Davemed Healthcare Co., Ltd. (529128716)

Establishment
Name	Address	ID/FEI	Business Operations
Davemed Healthcare Co., Ltd		529128716	manufacture(70897-010)