ANTISEPTIC DISINFECTANT

Manufacturer
Nano Care Deutschland AG
Effective date
2020-08-09
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:24:14

Label at a glance#

ProductANTISEPTIC DISINFECTANT
Active ingredientSILICON DIOXIDE
Label structure13 sections

Storage and handling

Store between 15-30C (59-86F) Avoid freezing and excessive heat above 40C (104F)

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

The liquid guard is manufactured using only the following United States Pharmacopoeia (USP) grade ingredients in the preparation of the product (percentage in final product formulation) consistent with World Health Organization (WHO) recommendations:

The firm does not add other active or inactive ingredients. Different or additional ingredients may impact the quality and potency of the product.

OTC - ACTIVE INGREDIENT SECTION

Silsesquioxane 2.9 % v/v. Purpose: Liquid Guard AntiSeptic

Antiseptic

OTC - PURPOSE SECTION

Antiseptic

INDICATIONS & USAGE SECTION

Liquid Guard Antiseptic to help reduce bacteria that potentially can cause disease.

WARNINGS SECTION

For external use only. Keep out of reach of eyes, ears, and mouth

OTC - DO NOT USE SECTION

Keep out of reach of children’s

OTC - WHEN USING SECTION

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

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.

DOSAGE & ADMINISTRATION SECTION

Place enough product to clean the infected area. Do not use of wet surfaces / skin.

STORAGE AND HANDLING SECTION

Store between 15-30C (59-86F)
Avoid freezing and excessive heat above 40C (104F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

purified water USP

Maximum 1000000000 mL in 1 CONTAINER (79836-510-01)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label ApprovedLabel Approved

5000 mL NDC: 79836-510-01

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
79836-510-012021-07-23C16284748780-1c7ccaba7-2abd-fd44-e053-dadaa90aa01bac31c0b7-76f3-7eeb-e053-2995a90a22a6

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79836-510-01ANTISEPTIC DISINFECTANT5000 mL in 1 BOTTLELIQUID50002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79836-510ANTISEPTIC DISINFECTANT (SILSESQUIOXANE) LIQUID [NANO CARE DEUTSCHLAND AG]2Legacy NDC, 1 package rows20200810_ac31c0b7-76f3-7eeb-e053-2995a90a22a6.zip

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79836-51079836-510-01

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
WATER059QF0KO0RIACT
SILICON DIOXIDEETJ7Z6XBU4ACTIB
METHYL ALCOHOLY4S76JWI15IACT

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
ac6dcc1b-eae4-1cc4-e053-2995a90aa9f0ac31c0b7-76f3-7eeb-e053-2995a90a22a62020-08-09WarningsExact identifier
spl id: ac6dcc1b-eae4-1cc4-e053-2995a90aa9f0
spl set id: ac31c0b7-76f3-7eeb-e053-2995a90a22a6

Reported adverse events (FAERS/openFDA)#

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