YMLABS- aloe hand sanitizer spray

YMLABS by

Drug Labeling and Warnings

YMLABS by is a Otc medication manufactured, distributed, or labeled by Yusef Manufacturing Laboratories. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

INDICATIONS & USAGE

DIRECTIONS: Spray a small amount into palm of hand.  Rub
together until dry.  If pump does not actuate, press and depress pump very slowly to prime.

WARNINGS

WARNINGS: For External Use Only. FLAMMABLE - Do not use near
heat, fire, flame or while smoking. *Do not store where temperature exceeds
105°F. Do not get in eyes. In case of eye contact flush with water. *Do not
Inhale or Ingest. If swallowed, get medical help or contact poison control
immediately. *Stop use and ask a doctor if skin irritation develops.
*KEEP OUT OF REACH OF CHILDREN.

KEEP OUT OF REACH OF CHILDREN

*KEEP OUT OF REACH OF CHILDREN.

ACTIVE INGREDIENT

Drug Facts

Active ingredients          Purpose

Ethyl Alcohol (62%).......Sanitizer

PURPOSE

USES: Decreases Bacteria on the hands.

INACTIVE INGREDIENT

INACTIVE INGREDIENTS: Water, Aloe Barbadensis Leaf Gel, Carbomer, Treithanolamine.

SPL UNCLASSIFIED SECTION

Made In USA
Distributed by
<Vendor, City, ST>
Questions? 877.827.5425
NEVER Tested On Animals.

Drug FactsActive ingredients Purpose Ethyl Alcohol (62%).......Sanitizer DIRECTIONS: Spray a small amount into palm of hand. Rubtogether until dry. If pump does not actuate, press and depress pump very slowly to prime.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

YMLABS 
aloe hand sanitizer spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 10827-1025
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	62 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CARBOMER HOMOPOLYMER TYPE A (UNII: F68VH75CJC)
TROLAMINE (UNII: 9O3K93S3TK)
ALOE VERA LEAF (UNII: ZY81Z83H0X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 10827-1025-1	30 g in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	12/30/2021
2	NDC: 10827-1025-2	59 g in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	12/30/2021
3	NDC: 10827-1025-3	9.5 g in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	12/30/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	12/30/2021

Labeler - Yusef Manufacturing Laboratories (144150674)

Registrant - Yusef Manufacturing Laboratories (144150674)

Establishment
Name	Address	ID/FEI	Business Operations
Yusef Manufacturing Laboratories		144150674	manufacture(10827-1025)