Alkaline Super Ionized Water

Manufacturer
Foshan Eric Biotechnology Co., Ltd.
Effective date
2020-06-08
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:13:11

Label at a glance#

ProductAlkaline Super Ionized Water
Active ingredientPOTASSIUM CARBONATE
Label structure8 sections

Label contents#

Full prescribing information#

DOSAGE & ADMINISTRATION SECTION

Store in a cool and dry place

INACTIVE INGREDIENT SECTION

Pure Water

INDICATIONS & USAGE SECTION

①Spray directly on the surface of the object and dry it or let dry naturally.

②dip the product with a paper towel and let dry naturally.

③spray directly on the surface of the food and rinse with water.

OTC - ACTIVE INGREDIENT SECTION

potassium carbonate

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of children

OTC - PURPOSE SECTION

Disinfection
Sterilization

WARNINGS SECTION

Please place it out of children's reach; if it goes into the eyes, please wash it with plenty of water until it is comfortable; if you drink it by mistake, please drink plenty of clear water. Not recommended for use on aluminum products and plated jewelry.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
41768-001-012022-01-28C16284748780-1d6a99b39-8d84-a426-e053-dadaa90af4c2a79dd0bd-9f93-70cf-e053-2a95a90a8366

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
41768-001-01Alkaline Super Ionized Water100 mL in 1 BOTTLESPRAY1001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
41768-001ALKALINE SUPER IONIZED WATER SPRAY [FOSHAN ERIC BIOTECHNOLOGY CO., LTD.]1Legacy NDC, 1 package rows20200609_a79dd0bd-9f93-70cf-e053-2a95a90a8366.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
41768-00141768-001-01

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
POTASSIUM CARBONATEBQN1B9B9HAACTIB
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
a79dd0bd-9f94-70cf-e053-2a95a90a8366a79dd0bd-9f93-70cf-e053-2a95a90a83662020-06-08WarningsExact identifier
spl id: a79dd0bd-9f94-70cf-e053-2a95a90a8366
spl set id: a79dd0bd-9f93-70cf-e053-2a95a90a8366

Reported adverse events (FAERS/openFDA)#

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