Antibacterial

Manufacturer: Brands International Corporation
Effective date: 2022-11-14
Label type: HUMAN OTC DRUG LABEL
Version: 5
Source: legacy-cache
Hydrated at: 2026-08-01 21:48:10

Label at a glance#

ProductAntibacterial Spring Rain

Active ingredientBENZALKONIUM CHLORIDE

Label structure10 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient - Benzalkonium Chloride - 0.13%

OTC - PURPOSE SECTION

Purpose - Antibacterial

INDICATIONS & USAGE SECTION

Use for handwashing to decrease bacteria on skin

WARNINGS SECTION

for external use only - hands only

OTC - WHEN USING SECTION

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

OTC - STOP USE SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DOSAGE & ADMINISTRATION SECTION

Direction

* wet hands

* apply to hands

* scrub thoroughly

* rinse thoroughly

INACTIVE INGREDIENT SECTION

Water, Sodium Laureth Sulfate, Cocamidopropyl Betaine, Sodium Chloride, Glycerin, Tetrasodium EDTA, Methylchloroisothiazolinone, Methylisothiazolinone, Yellow 5, Fragrance (Parfum), Polyquaternium-7, Citric acid.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

9B9

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 13 matching rows.

Antibacterial Spring Rain
Benzalkonium Chloride
EDETATE SODIUM
ALOE VERA LEAF
DIRECT BLUE 1
SODIUM CHLORIDE
METHYLCHLOROISOTHIAZOLINONE
WATER
SODIUM LAURETH SULFATE
COCAMIDOPROPYL BETAINE
METHYLISOTHIAZOLINONE
BENZALKONIUM
TOCOPHEROL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
50157-607	50157-607-44

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
EDETATE SODIUM	MP1J8420LU	IACT
ALOE VERA LEAF	ZY81Z83H0X	IACT
DIRECT BLUE 1	8NN34MAQ6H	IACT
SODIUM CHLORIDE	451W47IQ8X	IACT
METHYLCHLOROISOTHIAZOLINONE	DEL7T5QRPN	IACT
WATER	059QF0KO0R	IACT
SODIUM LAURETH SULFATE	BPV390UAP0	IACT
COCAMIDOPROPYL BETAINE	5OCF3O11KX	IACT
METHYLISOTHIAZOLINONE	229D0E1QFA	IACT
BENZALKONIUM CHLORIDE	F5UM2KM3W7	ACTIB
TOCOPHEROL	R0ZB2556P8	IACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
ed77b201-10df-363d-e053-2995a90a9975			ed77c1ec-3c1a-97a6-e053-2a95a90a08ab	2022-11-14	Warnings	Exact identifier spl id: ed77b201-10df-363d-e053-2995a90a9975 spl set id: ed77c1ec-3c1a-97a6-e053-2a95a90a08ab

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.