NOSK EX SLEEP- menthol liquid

Nosk EX Sleep by

Drug Labeling and Warnings

Nosk EX Sleep by is a Otc medication manufactured, distributed, or labeled by DreamAir Co.,. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

INGREDIENTS AND APPEARANCE

NOSK EX SLEEP 
menthol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70767-010
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Menthol (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	Menthol	0.2 g  in 10 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Alcohol (UNII: 3K9958V90M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70767-010-02	6 in 1 CARTON	05/01/2016
1	NDC: 70767-010-01	10 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	05/01/2016

Labeler - DreamAir Co., (689846965)

Registrant - DreamAir Co., (689846965)

Establishment
Name	Address	ID/FEI	Business Operations
DreamAir Co.,		689846965	manufacture(70767-010)