APTO SKINCARE Mandarin Hand Sanitizer

Mandarin Hand Sanitizer by

Drug Labeling and Warnings

Mandarin Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by APTO Skincare. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

MANDARIN HAND SANITIZER- alcohol gel 
APTO Skincare

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.

----------

APTO SKINCARE Mandarin Hand Sanitizer

Drug Facts

Active ingredient[s]

Alcohol 65%

Purpose Antiseptic

Use[s]

Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

For external use only. Flammable. Keep away from heat or flame

Do not use

on children less than 2 months of age

on open skin wounds

When using this product keep out of eyes, ears, and mouth. In case with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation or rash occurs. These maybe signs of a serious condition.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Use deliberately on hands, wrists and any other body surface that you wish to disinfect. Apply as many times as necessary - our clean and natural formulation is aggressive with germs and gentle with your skin.

Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

Store between 15-30C (59-86F)

Avoid freezing and excessive heat above 40C (104F)

Inactive ingredients deionized water, glycerin, hydroxyethylcellulose, propanediol, tocopheryl acetate, peg-7 glyceryl cocoate, aloe barbadensis extract, citrus nobilis (mandarin orange) peel oil

With 65% Alcohol, Aloe Vera & Vitamin E

Disinfecting

Purifying

Moisturizing

aptoskincare.com

Made in our factory in New Jersey, USA

Packaging

IMAGE

MANDARIN HAND SANITIZER 
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 79057-838
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL65 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D)  
PROPANEDIOL (UNII: 5965N8W85T)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
PEG-7 GLYCERYL COCOATE (UNII: VNX7251543)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
MANDARIN OIL (UNII: NJO720F72R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 79057-838-08237 mL in 1 BOTTLE; Type 0: Not a Combination Product05/22/202012/31/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A05/22/202012/31/2020
Labeler - APTO Skincare (086776880)

Revised: 1/2022
 

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.