Label: ZIPPITY DOOS SHIELD- rosemary liquid
-
Contains inactivated NDC Code(s)
NDC Code(s): 57240-2041-1 - Packager: Laurus Enterprises, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved homeopathic
DISCLAIMER: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.
Drug Label Information
Updated March 4, 2013
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredients
- Purpose
- Inactive Ingredients
- Application
- Caution
- PRINCIPAL DISPLAY PANEL - 249 mL Bottle Label
-
INGREDIENTS AND APPEARANCE
ZIPPITY DOOS SHIELD
rosemary liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:57240-2041 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Rosemary (UNII: IJ67X351P9) (Rosemary - UNII:IJ67X351P9) Rosemary 2.49 mg in 1 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Hydrogenated Castor Oil (UNII: ZF94AP8MEY) Tea Tree Oil (UNII: VIF565UC2G) Citronella Oil (UNII: QYO8Q067D0) Eucalyptus Oil (UNII: 2R04ONI662) Hamamelis Virginiana Top Water (UNII: NT00Y05A2V) Aloe Vera Leaf (UNII: ZY81Z83H0X) Panthenol (UNII: WV9CM0O67Z) Oxybenzone (UNII: 95OOS7VE0Y) Cocamidopropyl Betaine (UNII: 5OCF3O11KX) Triethyl Citrate (UNII: 8Z96QXD6UM) PEG/PPG-17/18 Dimethicone (UNII: 2E4ZJH3Z6R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:57240-2041-1 249 mL in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date Unapproved homeopathic 03/01/2010 Labeler - Laurus Enterprises, LLC (023220394)