Formology (as CMO) - ALL GOOD CITRUS HAND SANITIZER GEL, 72580-308

ALL GOOD CITRUS HAND SANITIZER by

Drug Labeling and Warnings

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

Drug Details [pdf]

ALL GOOD CITRUS HAND SANITIZER- ethyl alcohol gel 
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 CMO) - ALL GOOD CITRUS HAND SANITIZER GEL, 72580-308

ACTIVE INGREDIENT

ETHYL ALCOHOL 70% V/V

PURPOSE

ANTISEPTIC

USES

• FOR HAND WASHING TO DECREASE BACTERIA ON THE SKIN.
• RECOMMENDED FOR REPEATED USE.

WARNINGS

FOR EXTERNAL USE ONLY.

• FLAMMABLE
• KEEP AWAY FROM FIRE/FLAME.
• DO NOT USE THIS PRODUCT IN OR NEAR EYES IF CONTACT OCCURS RINSE THOROUGHLY WITH WATER.

• KEEP OUT OF REACH OF CHILDREN.
• CHILDREN UNDER 6 YEARS OF AGE SHOULD BE SUPERVISED WHEN USING THIS PRODUCT
• IN CASE OF ACCIDENTAL INGESTION, SEEK MEDICAL ASSISTANCE OR CONTACT A POISON CONTROL CENTER IMMEDIATELY.

DIRECTIONS

DISPENSE AN ADEQUATE AMOUNT IN YOUR PALM TO COVER ALL SURFACES OF HANDS COMPLETELY

• RUB HANDS TOGETHER UNTIL DRY
• DOES NOT REQUIRE RINSING.

OTHER INFORMATION

DO NOT STORE ABOVE 104°F/40°C.

• MAY DISCOLOR SOME FABRICS.

INACTIVE INGREDIENTS

AQUA, ALOE BARBADENSIS LEAF JUICE, GLYCERIN, HYDROXYETHYLCELLULOSE, CITRUS LIMON PEEL OIL.

ALL GOOD CITRUS HAND SANITIZER 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72580-308
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
ALOE VERA LEAF (UNII: ZY81Z83H0X)
GLYCERIN (UNII: PDC6A3C0OX)
HYDROXYETHYL CELLULOSE (100 MPA.S AT 2%) (UNII: R33S7TK2EP)
LEMON OIL (UNII: I9GRO824LL)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72580-308-11	100 mL in 1 TUBE; Type 0: Not a Combination Product	06/29/2020
2	NDC: 72580-308-12	1.5 mL in 1 PACKET; Type 0: Not a Combination Product	06/29/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	06/29/2020	06/01/2023

Labeler - Formology Lab Inc. (081102403)

Registrant - Formology Lab Inc. (081102403)

Establishment
Name	Address	ID/FEI	Business Operations
Formology Lab Inc.		081102403	manufacture(72580-308)

Revised: 1/2023

Document Id: f1f09f3e-ebe0-602a-e053-2995a90a77b5

34390-5

Set id: 150058f9-c2ff-46c9-a9ad-7b4822b23324

Version: 4

Effective Time: 20230110