Morisu
FDA Label NDC 75932-1001

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Kit Living Science Of Kyungnam College University Of Information & Technology for the product Morisu (NDC 75932-1001). 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 otc - active ingredient, inactive ingredient, otc - purpose, otc - keep out of reach of children, indications & usage, warnings, dosage & administration, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Otc - Active Ingredient

Active ingredient: adenosine

Inactive Ingredient

Inactive ingredient: Rooibos extract, black bean extract, black tea extract, mugwort extract, ylang ylang, rosemary, citric acid, anhydrous  ethanol, water, sodium hyaluronate,

Otc - Purpose

For hair grower and loss prevention

Otc - Keep Out Of Reach Of Children

Keep out of reach of the children

Indications & Usage

- spray on the scalp 2~3 times daily as needed- recommendable to apply enough on the scalp prior to going to bed

Warnings

- stop using and see a doctor if any hypersensitivity symptom continues- avoid storing under direct sung light or high temperature

Dosage & Administration

- for hair scalp spraying only

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