UCARE HAND SANITIZER- ethyl alcohol solution 
Open Door Packaging, Llc

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.

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ucare HAND SANITIZER

Drug Facts

Active ingredient[s]

Ethyl Alcohol 70% v/v

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 of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation or rash occurs. These may be 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

• Place enough product on hands to cover all surfaces. Rub hands together until dry.

• 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, carbomer, glycerin, triethanolamine

ucare FOUNDATION

Non-Sterile Solution

Moisturize your hands while decreasing bacteria.

usmooth

UNEXPECTED LUXURY

Springfield, MO 65803

Made in USA

usmooth.com

Packaging

IMAGEIMAGE

UCARE HAND SANITIZER 
ethyl alcohol solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:78086-905
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
GLYCERIN (UNII: PDC6A3C0OX)  
TROLAMINE (UNII: 9O3K93S3TK)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:78086-905-0260 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/23/2020
2NDC:78086-905-04118.3 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/28/2020
3NDC:78086-905-08236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/28/2020
4NDC:78086-905-85250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/28/2020
5NDC:78086-905-12354 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/28/2020
6NDC:78086-905-16473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/28/2020
7NDC:78086-905-641892 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/28/2020
8NDC:78086-905-283785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/28/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A05/23/2020
Labeler - Open Door Packaging, Llc (079129996)

Revised: 5/2020
Document Id: f676cb73-1a21-4e7d-bb10-e6515e789f20
Set id: 49df0c4d-5778-4018-a418-e1bef0c7b883
Version: 2
Effective Time: 20200528
 
Open Door Packaging, Llc