SIBARC

Manufacturer: JD corporation
Effective date: 2020-05-17
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:13:26

Label at a glance#

ProductSIBARC

Active ingredientHYPOCHLOROUS ACID

Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

hypochlorous acid

OTC - PURPOSE SECTION

sterilization, disinfection

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF THE CHILDREN

INDICATIONS & USAGE SECTION

take appropriate amount where needed

WARNINGS SECTION

■ Flammable. Keep away from fire or flame.

■ For external use only.

■ Do not use in eyes.

■ lf swallowed, get medical help promptly.

■ Stop use, ask doctor lf irritation occurs.

■ Keep out of reach of children.

DOSAGE & ADMINISTRATION SECTION

for external use only

INACTIVE INGREDIENT SECTION

water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
2362253	hypochlorous acid 0.005 % Topical Solution	PSN	1
2362253	hypochlorous acid 0.05 MG/ML Topical Solution	SCD	1
2362253	hypochlorous acid 0.005 % Topical Solution	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
75696-0002-1	2024-01-30	C162847	48780-1	1030e365-536a-111a-e063-dadaa90a10e2	Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
75696-0002-1	SIBARC	500 mL in 1 BOTTLE	LIQUID	500		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
75696-0002	SIBARC (HYPOCHLOROUS ACID) LIQUID [JD CORPORATION]	1	Legacy NDC, 1 package rows	20200518_a5d55e34-dac9-338f-e053-2995a90a01c1.zip

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

SIBARC
hypochlorous acid
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
75696-0002	75696-0002-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
HYPOCHLOROUS ACID	712K4CDC10	ACTIB

Source Document#

Source XML · Source PDF

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
a5d55e34-daca-338f-e053-2995a90a01c1			a5d55e34-dac9-338f-e053-2995a90a01c1	2020-05-17	Warnings	Exact identifier spl id: a5d55e34-daca-338f-e053-2995a90a01c1 spl set id: a5d55e34-dac9-338f-e053-2995a90a01c1

Reported adverse events (FAERS/openFDA)#

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