MISTTHIRTY

Manufacturer
Green Aroma
Effective date
2022-12-29
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:52:45

Label at a glance#

ProductMISTTHIRTY
Active ingredientHYPOCHLOROUS ACID
Label structure10 sections

Dosage and administration

If you use it once, spray 5 to 6 times on the hands and skin and gently touch several times. When used by children, please use it under the guardian's observation.

Storage and handling

Avoid direct sunlight, store in a cool and dry place.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Electrolyzed water (hypochlorous acid) (.002%)

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

DOSAGE & ADMINISTRATION SECTION

To help reduce bacteria that on the skin.

For use when soap and water are not available.

Warnings

WARNINGS SECTION

For external use only

When using this product

OTC - WHEN USING SECTION

Do not drink or inhale through the nose or mouth.

Stop use and ask a doctor

OTC - ASK DOCTOR SECTION

If you drank, drink plenty of water first, then consult a doctor.

Directions

INDICATIONS & USAGE SECTION

If you use it once, spray 5 to 6 times on the hands and skin and gently touch several times.

When used by children, please use it under the guardian's observation.

Other information

STORAGE AND HANDLING SECTION

Avoid direct sunlight, store in a cool and dry place.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Sodium Chloride

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

100ml NDC: 90054-201-01 Label100ml NDC: 90054-201-01 Label

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
90054-201-01MISTTHIRTY100 mL in 1 BOTTLE, SPRAYLIQUID1002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
90054-201MISTTHIRTY (HYPOCHLOROUS ACID) LIQUID [GREEN AROMA]2Legacy NDC, 1 package rows20221230_accce349-98a0-4b2a-e053-2995a90a45f9.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
90054-20190054-201-01

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
WATER059QF0KO0RIACT
HYPOCHLOROUS ACID712K4CDC10ACTIB
SODIUM CHLORIDE451W47IQ8XIACT

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
f1039d03-7cd0-4ecb-e053-2995a90a7841accce349-98a0-4b2a-e053-2995a90a45f92022-12-29WarningsExact identifier
spl id: f1039d03-7cd0-4ecb-e053-2995a90a7841
spl set id: accce349-98a0-4b2a-e053-2995a90a45f9

Reported adverse events (FAERS/openFDA)#

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