FDA.reportPublic FDA data

Nosk EX Sleep

Manufacturer
DreamAir Co.,
Effective date
2016-06-14
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:46:16

Label at a glance#

ProductNosk EX Sleep
Active ingredientMenthol
Label structure8 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient: Menthol 2.0%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Water, Alcohol, Glycerin, Dipropylene glycol, Gossypium Herbaceum(cotton) seed extract, Magnolia Kubus Bark extract, Lilium tigrinum extract, Paeonia albiflora root extract, Carbomer, Disodium EDTA, Triethanolamine

PURPOSE

OTC - PURPOSE SECTION

Purpose: Skin Refresher

Caution

WARNINGS SECTION

Caution: - For the external use only . - Do not apply to eyes ,wounds , broken skin and deep puncture wounds - For 7 years and older only. - When using this product do not get into eyes, Stop use and ask a doctor if rash occurs - Keep out of reach of children - It is recommend to stop applying and to talk to dermatologist immediately if you are suffering such conditions a rash, swell up and itchness - Do not leave it on high, low temperature or exposed on sunlight

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN

INDICATIONS & USAGE

INDICATIONS & USAGE SECTION

Indications and usage: 1. Apply to back of neckand, cervical vertebrae and shoulder , make you awake and refreshment. 2. Shake well up and down before use Push a little the ball on apply , liquid easily out.

DOSAGE & ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION

Dosage and administration: Take an adequate amount of this product.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1146695menthol 2 % Topical SolutionPSN1
1146695menthol 20 MG/ML Topical SolutionSCD1
1146695menthol 2 % Topical SolutionSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70767-010-022020-01-31C16284748780-19d75b9d0-413b-f424-e053-dadaa90a57ceab03a309-0957-4a26-9b2b-105cf58748c8

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70767-010-01Nosk EX Sleep10 mL in 1 BOTTLE, PLASTICLIQUID101
70767-010-02Nosk EX Sleep6 in 1 CARTONLIQUID61

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70767-010NOSK EX SLEEP (MENTHOL) LIQUID [DREAMAIR CO.,]1Legacy NDC, 2 package rows20160614_ab03a309-0957-4a26-9b2b-105cf58748c8.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
70767-01070767-010-01, 70767-010-02

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
MentholL7T10EIP3AACTIB
Water059QF0KO0RIACT
Alcohol3K9958V90MIACT

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
0f8bbb03-00ff-4581-8a0e-18181c16346aab03a309-0957-4a26-9b2b-105cf58748c82016-06-14WarningsExact identifier
spl id: 0f8bbb03-00ff-4581-8a0e-18181c16346a
spl set id: ab03a309-0957-4a26-9b2b-105cf58748c8

Reported adverse events (FAERS/openFDA)#

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