HAND CARE SET SPICED VANILLA- alcohol kit

Hand Care Set Spiced Vanilla by

Drug Labeling and Warnings

Hand Care Set Spiced Vanilla 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 Denat. 66%

Purpose

Antiseptic

Use

• For handwashing to decrease bacteria on the skin

Warnings

For external use only

• Flammable, Keep away from fire & flame
• Does not contain grain alcohol; do not drink. If taken internally will produce severe gastric disturbances

When using this product

• Avoid the eyes and mucous membranes 
• In the case of eyes or mucous membrane contact, rinse area thoroughly with water

Stop use and ask a doctor if 

• Condition worsens
• Redness or irritation develops
• Condition persist for more than 3 days

Keep out of reach of children. 

If swallowed, contact a doctor or 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

• Store below 105°F
• May discolor fabrics

Inactive ingredients:

Water, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, Fragrance. May Contain: FD&C Red No.4, FD&C Yellow No.5, FD&C Blue No.1, D&C Red No.33.

Questions?

Call 1-888-988-2427

Hand Care Set Spiced Vanilla (

62651-023-00)

Hand Sanitizer Spiced Vanilla, 1 oz (

62651-009-01)

INGREDIENTS AND APPEARANCE

HAND CARE SET SPICED VANILLA 
alcohol kit

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62651-023

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62651-023-00	1 in 1 KIT	10/15/2019

Quantity of Parts
Part #	Package Quantity	Total Product Quantity
Part 1	1 BOTTLE	29.5 mL

Part 1 of 1

HAND SANITIZER SPICED VANILLA 
alcohol gel

Product Information
Item Code (Source)	NDC: 62651-009
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	660 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
FD&C RED NO. 4 (UNII: X3W0AM1JLX)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62651-009-01	29.5 mL in 1 BOTTLE; Type 1: Convenience Kit of Co-Package

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	10/15/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	10/15/2019

Labeler - Base4 Ventures, LLC (137316126)