Nanoplus 007-01

Manufacturer
Nanoplus Technology Co., Limited
Effective date
2026-07-01
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
weekly-update
Hydrated at
2026-07-17 21:43:30

Label at a glance#

ProductOHTrust Mouth And Nasal Relief
Active ingredientHYDROXIDE ION
Label structure9 sections

Dosage and administration

Spray products 3-4 times directly into the back of the mouth and teeth or into nostril. Allow product to flow down the throat. Repeat when necessary.

Storage and handling

Store below 95˚F (35˚C).

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Hydroxide ions (544ppm)

Purpose

OTC - PURPOSE SECTION

Anti-bacterial

Use

INDICATIONS & USAGE SECTION

  • For mouth:

Kills bacteria and virus
Balance pH
Instant minty breath

  • For nasal:

Moisturizes and flushes irritants in nostrils

Relieves stuffy nose

Warnings

WARNINGS SECTION

  • Avoid contact with eyes. In case of contact, rinse eyes thoroughly with water immediately.
  • Use of this container by more than one person may spread infection.
  • Temporary discomforts such as burning, stinging, sneezing or an increase in nasal discharge may occur.
  • Stop use if rash or irritation develops. Do not drink it!

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children except under adult supervision.

Directions

DOSAGE & ADMINISTRATION SECTION

Spray products 3-4 times directly into the back of the mouth and teeth or into nostril. Allow product to flow down the throat. Repeat when necessary.

Other information

STORAGE AND HANDLING SECTION

Store below 95˚F (35˚C).

Inactive ingredients

INACTIVE INGREDIENT SECTION

Ultrapure water, Floviva Peppermint Oil (Mentha piperita) (100% Org PPAI)

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

007-01007-0130 mL NDC: 70970-007-01

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
70970-00770970-007-01

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
PEPPERMINT OILAV092KU4JHIACT
HYDROXIDE ION9159UV381PACTIB
WATER059QF0KO0RIACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
52025-02-10full-release2026-06-01 00:54:52

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
5cafd886-444e-2743-e063-6394a90a582bddad5680-7310-7c9c-e053-2995a90a5ba32026-09-30WarningsExact identifier
spl set id: ddad5680-7310-7c9c-e053-2995a90a5ba3

Reported adverse events (FAERS/openFDA)#

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