GLITTER RITZ GOLDEN VANILLA EMBERS- alcohol gel

Glitter Ritz Golden Vanilla Embers by

Drug Labeling and Warnings

Glitter Ritz Golden Vanilla Embers by is a Otc medication manufactured, distributed, or labeled by Landy International. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient                                     Purpose

Alcohol denat. 63% .................................. Antiseptic

PURPOSE

Uses

to decrease bacteria on the skin

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

INDICATIONS & USAGE

Hand Sanitizer

30 ml 1.0 fl.oz.

WARNINGS

Warnings

For external use only.

Flammable.

Keep away from heat and flame.

When using this product

• Avoid contact with eyes. If contact occurs, flush eyes with water.
• Avoid contact with broken skin.

Stop use and ask a doctor if

irritation and redness develop and persist for more than 72 hours.

DOSAGE & ADMINISTRATION

Directions

• Wet hands with product and allow to dry without wiping.
• Not recommended for infants.

INACTIVE INGREDIENT

Inactive Ingredients

alcohol denat., water, propylene glycol, acrylates/c10-30 alkyl acrylate crosspolymer, aminomethyl propanol, fragrance, lactose, cellulose, hydroxypropyl methylcellulose, jojoba esters, tocopheryl acetate, yellow 5 (CI 19140), red 4 (CI 14700)

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

GLITTER RITZ GOLDEN VANILLA EMBERS 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 51706-513
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	63   in 100 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
(C10-C30)ALKYL METHACRYLATE ESTER (UNII: XH2FQZ38D8)
AMINOMETHYL PROPANEDIOL (UNII: CZ7BU4QZJZ)
LACTOSE (UNII: J2B2A4N98G)
POWDERED CELLULOSE (UNII: SMD1X3XO9M)
HYPROMELLOSES (UNII: 3NXW29V3WO)
HYDROLYZED JOJOBA ESTERS (ACID FORM) (UNII: UDR641JW8W)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
FD&C RED NO. 4 (UNII: X3W0AM1JLX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 51706-513-01	63 g in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	04/15/2015

Labeler - Landy International (545291775)

Establishment
Name	Address	ID/FEI	Business Operations
Landy International		545291775	manufacture(51706-513)