Redu mineral

Manufacturer: AML Bio Co., Ltd.
Effective date: 2024-01-23
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: full-release
Hydrated at: 2026-06-01 00:07:46

Label at a glance#

ProductRedu mineral

Active ingredientWATER

Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

mineral complex

OTC - PURPOSE SECTION

corona virus

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF THE CHILDREN

INDICATIONS & USAGE SECTION

Take 3 times a day, 3cc at a time

WARNINGS SECTION

■ For external use only.

■ Do not use in eyes.

■ lf swallowed, get medical help promptly.

■ Stop use, ask doctor lf irritation occurs.

■ Keep out of reach of children.

DOSAGE & ADMINISTRATION SECTION

for external use only

INACTIVE INGREDIENT SECTION

Water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
91774e91-b249-45e3-8ff8-4b5db2927a69	Product name	1	20230718

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
81016-0005-1	Redu mineral	500 mL in 1 BOTTLE	LIQUID	500		3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
81016-0005	REDU MINERAL (MINERAL) LIQUID [AML BIO CO., LTD.]	3	Legacy NDC, 1 package rows	20240124_cbaeac99-b3ac-8eb2-e053-2a95a90ac863.zip

Products#

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

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

Redu mineral
mineral
WATER
ATORVASTATIN CALCIUM ANHYDROUS

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
81016-0005	81016-0005-1

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
Name	UNII	Kind
WATER	059QF0KO0R	ACTIB
ATORVASTATIN CALCIUM ANHYDROUS	C0GEJ5QCSO	IACT

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
0fa7fb97-12bc-2bfd-e063-6294a90a73bd			cbaeac99-b3ac-8eb2-e053-2a95a90ac863	2024-01-23	Warnings	Exact identifier spl id: 0fa7fb97-12bc-2bfd-e063-6294a90a73bd spl set id: cbaeac99-b3ac-8eb2-e053-2a95a90ac863

Reported adverse events (FAERS/openFDA)#

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