Nosk Ex Sleep
FDA Label NDC 70767-010

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Dreamair Co., for the product Nosk Ex Sleep (NDC 70767-010). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding active ingredient, inactive ingredient, purpose, caution, keep out of reach of children, indications & usage, dosage & administration, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

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.

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