HANNA DISINFECTANTspray

Manufacturer: Rainbow Co Ltd
Effective date: 2020-06-13
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:17:32

Label at a glance#

ProductHANNA DISINFECTANTspray

Active ingredientSODIUM HYPOCHLORITE

Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

sodium hypochlorite

INACTIVE INGREDIENT SECTION

WATER, peg-60 hydrogenated castor oil, aloe extract, camellia sinensis leaf extract, grapefruit seed extract, fragrance

OTC - PURPOSE SECTION

Sterilization of hands and skin

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF THE CHILDREN

INDICATIONS & USAGE SECTION

Apply an appropriate amount on your hands and rub well to dry.

WARNINGS SECTION

1. Do not use on the following body parts. A wide range of body parts and damaged skin around the eyes and ears, in the oral cavity (may have irritating effects)
2. If the following symptoms appear, stop using them immediately and consult a doctor or pharmacist.
1) Hypersensitivity symptoms such as rash, erythema, itching, and edema
2) Skin irritation symptoms

DOSAGE & ADMINISTRATION SECTION

for external use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label

Product Linked Resources#

Resource, Code type, Value table
Resource	Code type	Value	Equivalent identifiers	Source image
Barcode	EAN-13	8809317967790	GTIN-13: 8809317967790 EAN-13: 8809317967790 GTIN storage (14 digits): 08809317967790	label.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
74247-0014-1	2021-07-23	C162847	48780-1	c7ccaba7-145b-fd44-e053-dadaa90aa01b	Drug Facts
74247-0014-2	2021-07-23	C162847	48780-1	c7ccaba7-145b-fd44-e053-dadaa90aa01b	Drug Facts
74247-0014-3	2021-07-23	C162847	48780-1	c7ccaba7-145b-fd44-e053-dadaa90aa01b	Drug Facts
74247-0014-4	2021-07-23	C162847	48780-1	c7ccaba7-145b-fd44-e053-dadaa90aa01b	Drug Facts
74247-0014-5	2021-07-23	C162847	48780-1	c7ccaba7-145b-fd44-e053-dadaa90aa01b	Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
74247-0014-1	HANNA DISINFECTANTspray	55 mL in 1 BOTTLE	LIQUID	55	1
74247-0014-2	HANNA DISINFECTANTspray	300 mL in 1 BOTTLE	LIQUID	300	1
74247-0014-3	HANNA DISINFECTANTspray	500 mL in 1 BOTTLE	LIQUID	500	1
74247-0014-4	HANNA DISINFECTANTspray	2000 mL in 1 BOTTLE	LIQUID	2000	1
74247-0014-5	HANNA DISINFECTANTspray	5000 mL in 1 BOTTLE	LIQUID	5000	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
74247-0014	HANNA DISINFECTANTSPRAY (SODIUM HYPOCHLORITE) LIQUID [RAINBOW CO LTD]	1	Legacy NDC, 5 package rows	20200613_a7ee6281-8fda-7a28-e053-2995a90a05fd.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

HANNA DISINFECTANTspray
Sodium hypochlorite
GREEN TEA LEAF
GRAPEFRUIT PEEL
PEG-60 HYDROGENATED CASTOR OIL
ALOE VERA LEAF
WATER
HYPOCHLORITE ION

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
74247-0014	74247-0014-1, 74247-0014-2, 74247-0014-3, 74247-0014-4, 74247-0014-5

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
GREEN TEA LEAF	W2ZU1RY8B0	IACT
GRAPEFRUIT PEEL	3582N05Q44	IACT
PEG-60 HYDROGENATED CASTOR OIL	02NG325BQG	IACT
ALOE VERA LEAF	ZY81Z83H0X	IACT
WATER	059QF0KO0R	IACT
SODIUM HYPOCHLORITE	DY38VHM5OD	ACTIB

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
a7ee61ef-1c6f-ae55-e053-2a95a90af643			a7ee6281-8fda-7a28-e053-2995a90a05fd	2020-06-13	Warnings	Exact identifier spl id: a7ee61ef-1c6f-ae55-e053-2a95a90af643 spl set id: a7ee6281-8fda-7a28-e053-2995a90a05fd

Reported adverse events (FAERS/openFDA)#

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