FDA.reportPublic FDA data

LIQUIDGUARD

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 23:24:13

Label at a glance#

ProductLIQUIDGUARD
Active ingredientPHOSPHATE ION
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.

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Phosphates 2.5 % v/v. Purpose: Liquid Guard

OTC - PURPOSE SECTION

Liquid Guard

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

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

Do not use

OTC - DO NOT USE SECTION

Keep out od reach of childrens

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 (79836-500-01)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label ApprovedLabel Approved

5000 mL NDC: 79836-500-01

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
efd58dcf-540a-4531-8766-e713129ca6f2Product name120250307
4b7700e3-6e0e-45e5-9d22-6f754d61386eProduct name220250304
726062af-1135-4707-a1d7-57256991bbf9Product name220250226
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
19c71a3d-ed9c-166b-a7e5-38c250c35631Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
79836-500-012021-07-23C16284748780-1c7ccaba7-18ba-fd44-e053-dadaa90aa01bab81f320-c63b-05d7-e053-2995a90af4f5

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79836-500-01LIQUIDGUARD5000 mL in 1 BOTTLELIQUID50002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79836-500LIQUIDGUARD (PHOSPHATES) LIQUID [NANO CARE DEUTSCHLAND AG]2Legacy NDC, 1 package rows20200810_ab81f320-c63b-05d7-e053-2995a90af4f5.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
79836-50079836-500-01

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
NameUNIIKind
PHOSPHATE IONNK08V8K8HRACTIB
WATER059QF0KO0RIACT

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
ac752baf-6510-6deb-e053-2995a90a6748ab81f320-c63b-05d7-e053-2995a90af4f52020-08-09WarningsExact identifier
spl id: ac752baf-6510-6deb-e053-2995a90a6748
spl set id: ab81f320-c63b-05d7-e053-2995a90af4f5

Reported adverse events (FAERS/openFDA)#

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