NDC 48951-8076

Prunus

Prunus

Prunus is a Topical Liquid in the Human Otc Drug category. It is labeled and distributed by Uriel Pharmacy Inc.. The primary component is Sloe.

• Product ID: 48951-8076_6b123a75-e30f-653d-e053-2a91aa0a76de
• NDC: 48951-8076
• Product Type: Human Otc Drug
• Proprietary Name: Prunus
• Generic Name: Prunus
• Dosage Form: Liquid
• Route of Administration: TOPICAL
• Marketing Start Date: 2009-09-01
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Uriel Pharmacy Inc.
• Substance Name: SLOE
• Active Ingredient Strength: 1 [hp_X]/mL
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 48951-8076-6

125 mL in 1 BOTTLE, GLASS (48951-8076-6)

• Marketing Start Date: 2009-09-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 48951-8076-6 [48951807606]

Prunus LIQUID

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2009-09-01

Drug Details

Active Ingredients

Ingredient	Strength
SLOE	1 [hp_X]/mL

OpenFDA Data

• SPL SET ID: 252f0916-7212-4dc4-88ef-cb6664ccac1d
• Manufacturer:
  • Uriel Pharmacy Inc.
• UNII:
  • 3MLB4858X7