Formology (as PLD) - SUNYTIZER ALL PURPOSE HAND SANITIZING SPRAY - 70% ALCOHOL, 72580-310

ALL PURPOSE HAND SANITIZING by

Drug Labeling and Warnings

ALL PURPOSE HAND SANITIZING by is a Otc medication manufactured, distributed, or labeled by Formology Lab Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ALL PURPOSE HAND SANITIZING 70 PERCENT- ethyl alcohol spray 
Formology Lab Inc.

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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Formology (as PLD) - SUNYTIZER ALL PURPOSE HAND SANITIZING SPRAY - 70% ALCOHOL, 72580-310

ACTIVE INGREDIENT

ETHYL ALCOHOL 70% V/V

PURPOSE

ANTISEPTIC

USES

HAND AND SURFACES 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

• IN 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

• TO SANITIZE HANDS: SPRAY ENOUGH PRODUCT ON HANDS TO COVER 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

GLYCERIN, WATER (AQUA), ALOE BARBADENSIS LEAF JUICE, EUCALYPTUS OIL, BACKHOUSIA CITRODORA (LEMON MYRTLE) OIL.

QUESTIONS?

CALL TOLL-FREE 1-833-778-1690 OR VISIT WWW.SUNYTIZER.COM

ALL PURPOSE HAND SANITIZING  70 PERCENT
ethyl alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72580-310
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
EUCALYPTUS OIL (UNII: 2R04ONI662)
BACKHOUSIA CITRIODORA LEAF OIL (UNII: 2UQQ0PI06P)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72580-310-11	120 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/25/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	08/25/2020	07/31/2023

Labeler - Formology Lab Inc. (081102403)

Revised: 1/2023

Document Id: f1f09ca2-53e8-60e7-e053-2995a90aa2e3

34390-5

Set id: c2a21037-61b7-49f0-bae5-0672278f2c59

Version: 4

Effective Time: 20230110