Studio selection Antibacterial liquid hand soap- Golden

Antibacterial by

Drug Labeling and Warnings

Antibacterial by is a Otc medication manufactured, distributed, or labeled by Brands International Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ANTIBACTERIAL SPRING RAIN- benzalkonium chloride liquid 
Brands International Corporation

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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Studio selection Antibacterial liquid hand soap- Golden

Active Ingredient - Benzalkonium Chloride - 0.13%

Purpose - Antibacterial

Use for handwashing to decrease bacteria on skin

for external use only - hands only

When using this product avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water

Stop use and ask a doctor if irritation or redness develops.

keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately

Direction

* wet hands

* apply to hands

* scrub thoroughly

* rinse thoroughly

Water, Sodium Laureth Sulfate, Cocamidopropyl Betaine, Sodium Chloride, Glycerin, Tetrasodium EDTA, Methylchloroisothiazolinone, Methylisothiazolinone, Vitamin E, Blue# 1, Yellow 5, Fragrance (Parfum)

ANTIBACTERIAL  SPRING RAIN
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 50157-606
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1.3 mg  in 1000 mL

Inactive Ingredients
Ingredient Name	Strength
.ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
VAT YELLOW 4 (UNII: 8XO6A4G496)
FD&C RED NO. 40 (UNII: WZB9127XOA)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
EDETATE SODIUM (UNII: MP1J8420LU)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
WATER (UNII: 059QF0KO0R)
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 50157-606-44	443.6 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	11/14/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	11/14/2022

Labeler - Brands International Corporation (243748238)

Establishment
Name	Address	ID/FEI	Business Operations
Brands International Corporation		243748238	manufacture(50157-606)

Revised: 11/2022

Document Id: ed777946-e742-08e3-e053-2995a90aa88d

34390-5

Set id: ed777946-e741-08e3-e053-2995a90aa88d

Version: 4

Effective Time: 20221114