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Nosk EX Sleep

Dosage form: liquid
Ingredients: Menthol 0.2g in 10mL
Labeler: DreamAir Co.,
NDC Code: 70767-010

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

ACTIVE INGREDIENT

Active Ingredient: Menthol 2.0%

INACTIVE INGREDIENT

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

Purpose: Skin Refresher

Caution

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

KEEP OUT OF REACH OF CHILDREN

INDICATIONS & USAGE

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 and administration: Take an adequate amount of this product.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NOSK EX SLEEP 
menthol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70767-010
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Menthol (MENTHOL) Menthol0.2 g  in 10 mL
Inactive Ingredients
Ingredient NameStrength
Water 
Alcohol 
Packaging
#Item CodePackage Description
1NDC:70767-010-026 BOTTLE, PLASTIC in 1 CARTON
1NDC:70767-010-0110 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34805/01/2016
Labeler - DreamAir Co., (689846965)
Registrant - DreamAir Co., (689846965)
Establishment
NameAddressID/FEIOperations
DreamAir Co.,689846965manufacture(70767-010)

Revised: 06/2016
 
DreamAir Co.,

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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