SMART CARE ANTIBACTERIAL HANDSOAP- benzalkonium chloride liquid

Smart Care Antibacterial HANDSOAP by

Drug Labeling and Warnings

Smart Care Antibacterial HANDSOAP by is a Otc medication manufactured, distributed, or labeled by Ashtel Studios, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Benzalkonium chloride 0.2% w/w

Purpose

Antiseptic

Use

• For washing hands to decrease bacteria on hands

Warnings

For external use only

Do not use  on open skin wounds

When using this product  avoid contact with eyes. In case of eye contact, flush with water.

Stop use and ask a doctor if  irritation and redness develop

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Pump onto wet hands, vigorously work into a lather, and rinse thoroughly

Other information

• Store in a cool dry place below 104°F

Inactive ingredients

water, cocamidopropyl betaine, cocamidopropylamine oxide, lauryl glucoside, cocamide DEA, glycerin, PEG-150 distearate, fragrance, disodium EDTA, benzophenone-4, citric acid, sodium chloride, benzyl alcohol, methylchloroisothiazolinone, methylisothiazolinone, FD&C blue no. 1, FD&C yellow no. 5, FD&C yellow no. 6, ext. D&C violet no. 2, FD&C red no. 40

Questions or Comments?

1-877-274-8358 Toll Free in USA  1-909-434-0911 International

SPL UNCLASSIFIED SECTION

KILLS UP TO 99% OF MOST COMMON GERMS

CUCUMBER & TEA

LAVENDER

TROPICAL BEACH

SWEET PEACH

DISTRIBUTED BY ASHTEL STUDIOS INC. ONTARIO, CALIFORNIA 91761

PATENTS, COPYRIGHTS AND TRADEMARKS GRANTED OR PENDING WORLDWIDE

DESIGNED IN USA  MADE IN CHINA

Packaging

INGREDIENTS AND APPEARANCE

SMART CARE ANTIBACTERIAL HANDSOAP 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70108-071
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.1809 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
COCAMIDOPROPYLAMINE OXIDE (UNII: M4SL82J7HK)
LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)
COCO DIETHANOLAMIDE (UNII: 92005F972D)
GLYCERIN (UNII: PDC6A3C0OX)
PEG-150 DISTEARATE (UNII: 6F36Q0I0AC)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
SULISOBENZONE (UNII: 1W6L629B4K)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
BENZYL ALCOHOL (UNII: LKG8494WBH)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
EXT. D&C VIOLET NO. 2 (UNII: G5UX3K0728)
FD&C RED NO. 40 (UNII: WZB9127XOA)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70108-071-01	400 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	01/13/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	01/13/2021

Labeler - Ashtel Studios, Inc (148689180)