Active Ingredient
Alcohol 20%
D S
FDA Label NDC 74041-002
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Foshan Muzar Cosmetics Co., Ltd for the product D S (NDC 74041-002). 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, purpose, uses, warnings, when using this product, directions, other information, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antimicrobial
Uses
disinfection spray to help reduce bacteria on skin.
Warnings
Flammable.Keep away from fire or flame.For external use only.
When Using This Product
do not use in or near the eyes.In case of contact,rinse eyes thoroughly with water.Stop use and ask doctor if irritation or rash appears and SANITIZER lasts.Keep out of reach for children.If swallowed,get medical help or contact a With Vitamin E& Poison Control Center right away.
Directions
Place enough Product in your palm to thoroughly spread on both hands and rub into the skin until dry.
Children under 6 years of age should be supervised when using this product.
Other Information
Store below 106°F.(41°C)
May discolor certain fabrics or surfaces
Inactive Ingredients
Water,ARTEMISIA ARGYI leaf extract, EUCALYPTUS GLOBULUS leaf oil lavender(LAVANDULA ANGUSTIFOLIA) oil
ethanol,grapefruit(CITRUS ol,cedar(CEDRUS DEODARA) wood oil,Lonicera japonica Flower extract, propylene glycol,tea(CAMELLIA SINENSIS) leaf extract, butanediol,polyaminopropyi biguanide, phenoxyethanol, benzalkonium DISINFECTION SPRAY chioride,
ethylhexy! glycero.
* Please review the disclaimer below.
