OHTrust Nano Ion Water

Product NDC: 70970-006
Requested package NDC: 70970-006-01
11-digit product format: 709700006
Labeler code: 70970
Product ID: 70970-006_d4f87129-e92a-f5d5-e053-2a95a90ad1da
Type: HUMAN OTC DRUG
Nonproprietary name: Hydroxide Ions
Dosage form: LIQUID
Route: TOPICAL
Labeler: Nanoplus Life Biomedical Technology Co. Ltd.
Marketing category: UNAPPROVED DRUG OTHER
Marketing start: 2020-11-23
Marketing end: 0000-00-00
Substance: HYDROXIDE ION
Active strength: 0 g/100mL
NDC exclude flag: No
Listing certified through: 2023-12-31
Current FDA listing: Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	70970-006	70970-006-01	D	Discontinued by firm		2026-10-05

Reported adverse events (FAERS/openFDA)#

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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
70970-006-01	OHTrust Nano Ion Water	60 mL in 1 BOTTLE, SPRAY	LIQUID	60	5
70970-006-02	OHTrust Nano Ion Water	1000 mL in 1 BOTTLE, PUMP	LIQUID	1000	5
70970-006-03	OHTrust Nano Ion Water	5000 mL in 1 BOTTLE, PLASTIC	LIQUID	5000	5
70970-006-04	OHTrust Nano Ion Water	20000 mL in 1 PAIL	LIQUID	20000	5
70970-006-05	OHTrust Nano Ion Water	1000 mL in 1 BOTTLE, PLASTIC	LIQUID	1000	5

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
70970-006	OHTRUST NANO ION WATER (HYDROXIDE IONS) LIQUID [NANOPLUS LIMITED (CAYMAN) TAIWAN BRANCH]	5	Legacy NDC, 5 package rows	20250212_b4c08737-e877-a0d8-e053-2995a90a9efd.zip

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
OHTrust Nano Ion Water	HYDROXIDE IONS	Nanoplus Technology Co., Limited	b4c08737-e877-a0d8-e053-2995a90a9efd	2026-07-01	Warnings	Exact identifier ndc (package): 70970-006-01 ndc (product): 70970-006 ndc11 (package): 70970000601

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
9159UV381P	HYDROXIDE ION	14280-30-9	HYDROXIDE ION

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
70970-006-01	70970000601	60 mL in 1 BOTTLE, SPRAY (70970-006-01)	60 ml	2020-11-23	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Nanoplus 006-01, 02, 03, 04, 05	Nanoplus Technology Co., Limited	2026-07-01	HUMAN OTC DRUG LABEL	6