BLUE SANDALWOOD- hand sanitizer spray

Blue Sandalwood by

Drug Labeling and Warnings

Blue Sandalwood by is a Otc medication manufactured, distributed, or labeled by Bell International Laboratories, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Ethyl Alcohol 70% v/v

Purpose

Antiseptic

Uses

• To decrease bacteria on the skin
• Recommended for repeated use

Warnings

For external use only

Flammable, keep away from fire or flame

Do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water. Avoid contact with broken skin

Stop use and ask a doctor

• if irritation and redness develop
• Condition persists for more than 72 hours

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away

Directions

Place enough product in your palm to thoroughly cover your hands

Children under 6 years of age should be supervised when using this product

Rub hands together briskly until dry

Other Information

Protect the product in this container from excessive heat and direct sun

Store below 104F (40C)

May discolor certain fabrics

Inactive Ingredients

Water, Aloe Barbadensis Leaf Juice, Leuconostoc/Radish Root Ferment Lysate Filtrate, Glycereth-26, Citrus Limon (Lemon) Peel Oil, Citrus Aurantifolia (Lime) Oil, Fragrance, blue 1

pouch label

back label

INGREDIENTS AND APPEARANCE

BLUE SANDALWOOD 
hand sanitizer spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76150-273
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
GLYCERETH-26 (UNII: NNE56F2N14)
LEUCONOSTOC/RADISH ROOT FERMENT FILTRATE (UNII: D2QHA03458)
LEMON OIL (UNII: I9GRO824LL)
LIME OIL (UNII: UZH29XGA8G)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76150-273-51	30 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	07/01/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	07/01/2021

Labeler - Bell International Laboratories, Inc (967781555)