Label: GLITTER RITZ ICED BERRY- alcohol gel
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Contains inactivated NDC Code(s)
NDC Code(s): 51706-512-01 - Packager: Landy International
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated April 17, 2015
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- WARNINGS
- DOSAGE & ADMINISTRATION
- INACTIVE INGREDIENT
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
GLITTER RITZ ICED BERRY
alcohol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:51706-512 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:51706-512-01 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(51706-512)