SMOKE AND MIRRORS HAND SANITIZER COCONUT VANILLA- ethyl alcohol gel

Smoke and Mirrors Hand Sanitizer Coconut Vanilla by

Drug Labeling and Warnings

Smoke and Mirrors Hand Sanitizer Coconut Vanilla by is a Otc medication manufactured, distributed, or labeled by Pearl World Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Ethyl Alcohol 70%

Purpose

Antiseptic

Uses

To decrease bacteria on the skin that could cause disease. When water, soap and towel are not available. Recommended for repeated use.

Warnings

For external use only: hands.

Flammable. Keep away from fire or flame.

When using this product Keep out of eyes, ears, or mouth.  In case of eye contact, flush eyes thoroughly with water.  Avoid contact with broken skin.  Do not inhale or ingest.

Stop use and ask a doctor if Redness or irritation develop. Condition persists for more than 72 hours.

Keep out of reach of children Children should be supervised by an adult when using this product. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Wet hands thoroughly with product and allow to dry without wiping. No rinsing required. For children under 6, use only under adult supervision. Not recommended for infants.

Other information

 Store below 105°F (40°C).  May discolor certain fabrics. Harmful to wood finishes & plastics.

Inactive ingredients:

Water (Aqua), Carbomer, Triethanolamine, Aloe Barbadensis Extract, Glycerin, Propylene Glycol, Fragrance.
May Contain: FD & C Red 33 (CI 17200), FD & C Blue 1 (CI 42090), FD & C Yellow 5 (CI 19140), FD & C Yellow 6 (CI 15985).

SPL UNCLASSIFIED SECTION

• KILLS 99.9% OF GERMS

• 70% ALCOHOL

Manufactured for and distributed by

Pearl World Inc, NY, NY 10019

Pearlworldinc.com All rights reserved.

Designed in the USA. Made in China.

Packaging

INGREDIENTS AND APPEARANCE

SMOKE AND MIRRORS HAND SANITIZER COCONUT VANILLA 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69933-905
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
WATER (UNII: 059QF0KO0R)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
TROLAMINE (UNII: 9O3K93S3TK)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)

Other Ingredients
Ingredient Kind	Ingredient Name	Quantity
May contain	D&C RED NO. 33 (UNII: 9DBA0SBB0L)
May contain	FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
May contain	FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
May contain	FD&C YELLOW NO. 6 (UNII: H77VEI93A8)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69933-905-32	30 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/08/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	06/08/2023

Labeler - Pearl World Inc. (043130142)