PENACOM Hypochlorous acid disinfectant

Manufacturer
Shenzhen Qianhai PENACLO Biotechnology Co., Ltd
Effective date
2021-04-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:39:25

Label at a glance#

ProductPENACOM Hypochlorous acid disinfectant
Active ingredientHYPOCHLOROUS ACID
Label structure12 sections

Dosage and administration

1.Ardisinfection:Spray PENACOM direct yorwthairpurfier eliminate polution sources, without dition, keep the effected space closed, spray evenly in all directions according to the usage amount of 5ml PENACOM peronemin the actual space. 2.Skindsifecion:Spray PENACOM with appropriate amount on the affected area, and let the area dry naturaly. 3.Surface disinfect on:Evenly wipe or spray PENACOM with appropriate amount...

Storage and handling

Keep in cool and dy place away from ght Use the product with in 60 days after the first opening.The surface contaminant should be removed before dsinfecing.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Hypochlorous acid ENACLO factor) 0.01%

Purpose

OTC - PURPOSE SECTION

disinfection

Use

INDICATIONS & USAGE SECTION

Applicable to disinfection of air, skin surface, object surface, mucosa, fruit and vegetables, and fabric surface.

Warnings

WARNINGS SECTION

For extermal use only, do not use of you are alergic to Hypochlorous acid or Borneolum

When using this produc, do not take toraly, in case of acidental contact with eyes, rinse eyes thoroughy with water

Stop use and ask a doctor if it at on or rash occurs. Keep out of reach of children.
Use diecty, do not combine the product wth other detergents, disinfectants etc.

Do not use

OTC - DO NOT USE SECTION

For extermal use only, do not use of you are alergic to Hypochlorous acid or Borneolum

When using this produc, do not take toraly, in case of acidental contact with eyes, rinse eyes thoroughy with water

Use diecty, do not combine the product wth other detergents, disinfectants etc.

OTC - WHEN USING SECTION

When using this produc, do not take toraly, in case of acidental contact with eyes, rinse eyes thoroughy with water

Stop use and ask a doctor if it at on or rash occurs. Keep out of reach of children.
Use diecty, do not combine the product wth other detergents, disinfectants etc.

OTC - STOP USE SECTION

Stop use and ask a doctor if it at on or rash occurs.
Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.
Use diecty, do not combine the product wth other detergents, disinfectants etc.

Directions

DOSAGE & ADMINISTRATION SECTION

1.Ardisinfection:Spray PENACOM direct yorwthairpurfier eliminate polution sources, without dition, keep the effected space closed, spray evenly in all directions according to the usage amount of 5ml PENACOM peronemin the actual space.
2.Skindsifecion:Spray PENACOM with appropriate amount on the affected area, and let the area dry naturaly.
3.Surface disinfect on:Evenly wipe or spray PENACOM with appropriate amount on the surface of affected object, and rinse them with dean water or let the m dry natura y after 5 minutes of processing.
4.Mucosal dsn fect on:Take appropriate amount of PENACOM dre cty on the oral mucosa, nasal mucosa, vaginal mucosa.
5.Fruts and vegetables diifeci on:Spray appropriate amount of PENA COM on the surface of fruits and vegetables or soakt for 10 minutes, then clean it with clean water
6.Fabric surface dsn fection:Spray appropriate amount of PENACOM on the surface of the fabrc for 15 minutes.

Other information

STORAGE AND HANDLING SECTION

Keep in cool and dy place away from ght Use the product with in 60 days after the first opening.The surface contaminant should be removed before dsinfecing.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Purified water, Borneolum.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LABEL81763-001-01 100ml

LABEL81763-001-01 100mlLABEL81763-001-01 100ml

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2721462hypochlorous acid 0.01 % Topical SprayPSN1
2721462hypochlorous acid 0.1 MG/ML Topical SpraySCD1
2721462hypochlorous acid 0.01 % Topical SpraySY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
81763-001-012022-07-29C16284748780-1e4f33bdf-ad9d-d8a0-e053-dadaa90a6e4e81763-001 PENACOM Hypochlorous acid disinfectant

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
81763-001-01PENACOM Hypochlorous acid disinfectant100 mL in 1 BOXSPRAY1001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
81763-001PENACOM HYPOCHLOROUS ACID DISINFECTANT SPRAY [SHENZHEN QIANHAI PENACLO BIOTECHNOLOGY CO., LTD]1Legacy NDC, 1 package rows20210403_bef441ed-0e9b-4140-e053-2995a90a81dd.zip

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81763-00181763-001-01

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
NameUNIIKind
BORNEOLM89NIB437XIACT
WATER059QF0KO0RIACT
HYPOCHLOROUS ACID712K4CDC10ACTIB

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
bef441ed-0e8d-4140-e053-2995a90a81ddbef441ed-0e9b-4140-e053-2995a90a81dd2021-04-01WarningsExact identifier
spl id: bef441ed-0e8d-4140-e053-2995a90a81dd
spl set id: bef441ed-0e9b-4140-e053-2995a90a81dd

Reported adverse events (FAERS/openFDA)#

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