NDC 57240-2041

Zippity Doos SHIELD

Rosemary

Zippity Doos SHIELD is a Topical Liquid in the Human Otc Drug category. It is labeled and distributed by Laurus Enterprises, Llc. The primary component is Rosemary.

• Product ID: 57240-2041_394d0c56-a4b2-4acd-8977-ef591a007405
• NDC: 57240-2041
• Product Type: Human Otc Drug
• Proprietary Name: Zippity Doos SHIELD
• Generic Name: Rosemary
• Dosage Form: Liquid
• Route of Administration: TOPICAL
• Marketing Start Date: 2010-03-01
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Laurus Enterprises, LLC
• Substance Name: ROSEMARY
• Active Ingredient Strength: 2 mg/mL
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 57240-2041-1

249 mL in 1 BOTTLE (57240-2041-1)

• Marketing Start Date: 2010-03-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 57240-2041-1 [57240204101]

Zippity Doos SHIELD LIQUID

• Marketing Category: Unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2010-03-01
• Inactivation Date: 2019-11-27

Drug Details

Active Ingredients

Ingredient	Strength
ROSEMARY	2.49 mg/mL

OpenFDA Data

• SPL SET ID: e47df67d-61f0-472e-8dfb-f19f1baf21a7
• Manufacturer:
  • Laurus Enterprises, LLC
• UNII:
  • IJ67X351P9

NDC Crossover Matching brand name "Zippity Doos SHIELD" or generic name "Rosemary"

NDC	Brand Name	Generic Name
57240-2027	Zippity Doos	Rosemary
57240-2041	Zippity Doos	Rosemary