EMHS 1 HAND SANITIZER- isopropyl alcohol gel 
Sayida Group

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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EMHS1 Hand Sanitizer (1L - no pump) NDC: 77858-0755-1
EMHS1 Hand Sanitizer (1L - pump) NDC: 77858-0755-2

Active Ingredient(s)

Isopropyl Alcohol 75% v/v.

Purpose

Antiseptic

Use

To help reduce bacteria that potentially can cause disease.

Warnings

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

Do not use

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.

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

Directions

Other information

Inactive ingredients

carbomer, citrus oil, fragrance, glycerin, rosemary oil, triethanolamine, water

Side Panel

Without rinsing. Non-sticky formula. Disinfecting anti-bacterial gel.

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.

WARNINGS: For external use only. Flammable. Keep away from heat or flame. Do not use on children less than 2 months of age or on open skin wounds. Keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water. Stop use if rash or irritation occurs. Keep out of the reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Distributed by: Sayida Group LLC

6538 Collins Ave #401

Miami Beach, FL33141

www.emhs1.com

Made In Mexico

Package Label - Principal Display Panel

Distributed by Sayida Group

6538 Collins Ave #401

Miami Beach, FL 33141

EMHS1 Hand Sanitizer (1L - no pump) NDC: 77858-0755-1

EMHS1 Hand Sanitizer (1L - pump) NDC: 77858-0755-2

isop

EMHS 1 HAND SANITIZER 
isopropyl alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:77858-0755
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL75 L  in 100 L
Inactive Ingredients
Ingredient NameStrength
GLYCERIN (UNII: PDC6A3C0OX)  
WATER (UNII: 059QF0KO0R)  
ROSEMARY OIL (UNII: 8LGU7VM393)  
TROLAMINE (UNII: 9O3K93S3TK)  
CARBOMER 1342 (UNII: 809Y72KV36)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:77858-0755-11 L in 1 BOTTLE; Type 0: Not a Combination Product06/26/2020
2NDC:77858-0755-21 L in 1 BOTTLE, PUMP; Type 0: Not a Combination Product06/26/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A06/26/2020
Labeler - Sayida Group (117520711)

Revised: 6/2020
Document Id: a90336f9-7169-8265-e053-2995a90ab12a
Set id: a902e9e8-7762-0a9c-e053-2a95a90ac56c
Version: 2
Effective Time: 20200626
 
Sayida Group