SANITIZING WIPES WITH ALOE GRAPEFRUIT GROVE- alcohol cloth

Sanitizing wipes with aloe Grapefruit Grove by

Drug Labeling and Warnings

Sanitizing wipes with aloe Grapefruit Grove by is a Otc medication manufactured, distributed, or labeled by The Honest Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Ethyl Alcohol 65%

Purpose

Antiseptic

Uses

• Helps reduce bacteria on the skin 
• Recommended for repeated use

Warnings

For external use only. Flammable, keep away from fire, sparks, and sources or ignition.

When using this product

• Keep out of eyes 
• In case of contact with eyes, flush thoroughly with water

Stop use and ask a doctor if

irritation and redness develop and persist for more than 72 hours

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center immediately.

Directions

• Wipe hands thoroughly with product when there's no soap and water around. Discard after use, please don't flush.
• For children under 6, use adult supervision

Other Information

• Do not store above 104°F/40°C 
• Not for use as a baby wipe
• Do not use in genital area or on damaged skin

Inactive ingredients

Aloe Barbadensis Leaf Extract, Citrus Paradisi (Grapefruit) Peel Oil, Ethyl Butyrate, Ethyl Hydroxypyrone, Furaneol, Gamma-Undecalactone, Glycerin, Grapefruit Mercaptan, Limonene, Methylbenzyl Acetate, Neral, Triethyl Citrate, Water

Package Labeling:69366-317-25

Package Labeling:69366-317-26

Package Labeling:69366-317-24

INGREDIENTS AND APPEARANCE

SANITIZING WIPES WITH ALOE GRAPEFRUIT GROVE 
alcohol cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69366-317
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	65 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
GRAPEFRUIT OIL (UNII: YR377U58W9)
ETHYL BUTYRATE (UNII: UFD2LZ005D)
ETHYL MALTOL (UNII: L6Q8K29L05)
DIMETHYLHYDROXY FURANONE (UNII: 20PI8YZP7A)
.GAMMA.-UNDECALACTONE (UNII: QB1T0AG2YL)
GLYCERIN (UNII: PDC6A3C0OX)
1-P-MENTHENE-8-THIOL (UNII: 7AT54D0N8R)
LIMONENE, (+)- (UNII: GFD7C86Q1W)
METHYLBENZYL ACETATE (UNII: P4RVP859F5)
NERAL (UNII: 8M466BQL1X)
TRIETHYL CITRATE (UNII: 8Z96QXD6UM)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69366-317-26	15 in 1 POUCH	05/01/2022
1		4.32 mL in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
2	NDC: 69366-317-24	50 in 1 POUCH	05/01/2022	06/30/2024
2		4.32 mL in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
3	NDC: 69366-317-25	3 in 1 PACKAGE	05/01/2022	06/30/2024
3		50 in 1 POUCH
3		4.32 mL in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	05/01/2022

Labeler - The Honest Company (969962757)