76836-001_Daily Doctor Sterilization Spray Plus

Manufacturer: GFC Life Science Co., Ltd.
Effective date: 2020-05-01
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:09:15

Label at a glance#

ProductDaily Doctor Sterilization Plus

Active ingredientSODIUM HYPOCHLORITE

Label structure7 sections

Dosage and administration

Use as liquid. Sterilize by immersing completely for about 3 to 5 minutes. For instruments that are difficult to deposit, spray and sterilize for about 3 minutes before wiping off.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Sodium Hypochlorite 0.2%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Use

INDICATIONS & USAGE SECTION

Prevent and treat infection of the skin

Warnings

WARNINGS SECTION

For external use only

OTC - WHEN USING SECTION

Do not use if sensitive of chlorine compounds.

OTC - STOP USE SECTION

Stop use and ask a doctor if redness, irritation or swelling or pain persists or increases.

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 right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Use as liquid. Sterilize by immersing completely for about 3 to 5 minutes. For instruments that are difficult to deposit, spray and sterilize for about 3 minutes before wiping off.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Hydrochloric acid

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Product Label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
76836-001-01	2022-01-28	C162847	48780-1	d6a99b39-a49b-a426-e053-dadaa90af4c2	76836-001_Daily Doctor Sterilization Spray Plus
76836-001-02	2022-01-28	C162847	48780-1	d6a99b39-a49b-a426-e053-dadaa90af4c2	76836-001_Daily Doctor Sterilization Spray Plus

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
76836-001-01	Daily Doctor Sterilization Plus	60 mL in 1 BOTTLE, SPRAY	SPRAY	60		1
76836-001-02	Daily Doctor Sterilization Plus	500 mL in 1 BOTTLE, SPRAY	SPRAY	500		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
76836-001	DAILY DOCTOR STERILIZATION PLUS (SODIUM HYPOCHLORITE) SPRAY [GFC LIFE SCIENCE CO., LTD.]	1	Legacy NDC, 2 package rows	20200502_705a3db5-bfe2-4f2c-80ca-a71b70642f05.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

Daily Doctor Sterilization Plus
SODIUM HYPOCHLORITE
WATER
HYDROCHLORIC ACID
HYPOCHLORITE ION

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
76836-001	76836-001-01, 76836-001-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
HYDROCHLORIC ACID	QTT17582CB	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
a49a51ee-9901-3675-e053-2a95a90aca85			705a3db5-bfe2-4f2c-80ca-a71b70642f05	2020-05-01	Warnings	Exact identifier spl id: a49a51ee-9901-3675-e053-2a95a90aca85 spl set id: 705a3db5-bfe2-4f2c-80ca-a71b70642f05

Reported adverse events (FAERS/openFDA)#

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