HAND SANITIZER COCONUT DREAMS- alcohol gel

Hand Sanitizer Coconut Dreams by

Drug Labeling and Warnings

Hand Sanitizer Coconut Dreams by is a Otc medication manufactured, distributed, or labeled by Base4 Ventures, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Alcohol 62%

Purpose

Antimicrobial

Use

hand sanitizer to help decrease bacteria on the skin

Warnings

For external use only.

Flammable. Keep away from heat and flame.

When using this product

• keep away from eyes. If contact, rinse eyes thoroughly with water.

Stop use and ask a doctor if 

• redness or irritation develops and issues persist seek medical attention.

Keep out of reach of children. 

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

Directions

• rub dime sized amount between hands until dry
• supervise children in the use of this product
• in the case of eye contact rinse eyes thoroughly with water

Other information

• Do not store above 105°F
• may discolor some fabrics

Inactive ingredients:

Water, Glycerin, PEG-40 Hydrogenated Castor Oil, Carbomer, Phenoxyethanol, Benzyl Alcohol, Fragrance, Sodium Hydroxide, May Contain: FD&C Yellow No.5, FD&C Red No.4, D&C Red No.33, FD&C Blue No.1.

Package Labeling:

INGREDIENTS AND APPEARANCE

HAND SANITIZER COCONUT DREAMS 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62651-018
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	620 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
BENZYL ALCOHOL (UNII: LKG8494WBH)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62651-018-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	10/01/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	10/01/2019

Labeler - Base4 Ventures, LLC (137316126)