NDC 60986-1011

Rubus

Rubus Fruticosus, Iris Germanica, Vaccinium Myrtillus, Syzygium Jambolanum, Okoubaka Aubrevillei

Rubus is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Marco Pharma International Llc.. The primary component is Blackberry; Iris Germanica Root; Bilberry; Syzygium Cumini Seed; Okoubaka Aubrevillei Bark.

• Product ID: 60986-1011_8bb74f2e-11d3-4428-89c2-be3df15bbbf5
• NDC: 60986-1011
• Product Type: Human Otc Drug
• Proprietary Name: Rubus
• Generic Name: Rubus Fruticosus, Iris Germanica, Vaccinium Myrtillus, Syzygium Jambolanum, Okoubaka Aubrevillei
• Dosage Form: Liquid
• Route of Administration: ORAL
• Marketing Start Date: 1992-03-01
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Marco Pharma International LLC.
• Substance Name: BLACKBERRY; IRIS GERMANICA ROOT; BILBERRY; SYZYGIUM CUMINI SEED; OKOUBAKA AUBREVILLEI BARK
• Active Ingredient Strength: 2 [hp_X]/100mL; [hp_X]/100mL; [hp_X]/100mL; [hp_X]/100mL; [hp_X]/100mL
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 60986-1011-3

50 mL in 1 BOTTLE, GLASS (60986-1011-3)

• Marketing Start Date: 1992-03-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 60986-1011-3 [60986101103]

Rubus LIQUID

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 1992-03-01
• Inactivation Date: 2019-11-13

NDC 60986-1011-4 [60986101104]

Rubus LIQUID

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 1992-03-01
• Inactivation Date: 2019-11-13

Drug Details

Active Ingredients

Ingredient	Strength
BLACKBERRY	2 [hp_X]/100mL

OpenFDA Data

• SPL SET ID: bcaf8cd2-3880-4dd7-9895-d33e63c1a229
• Manufacturer:
  • Marco Pharma International LLC.
• UNII:
  • 8A6OMU3I8L
  • 9P2U39H18W
  • 820LSF646I
  • MK2074187Z