NDC 60512-6010

PSORIASIS REAL RELIEF

Sulphur, Arsenicum Album, Alumen, Magnesia Sulphuricum, Natrum Sulphuricum

PSORIASIS REAL RELIEF is a Oral Tablet, Chewable in the Human Otc Drug category. It is labeled and distributed by Homeolab Usa Inc. The primary component is Sulfur; Arsenic Trioxide; Potassium Alum; Magnesium Sulfate Heptahydrate; Sodium Sulfate.

• Product ID: 60512-6010_7a89dc56-e0f8-474c-8db5-4c3b37464df5
• NDC: 60512-6010
• Product Type: Human Otc Drug
• Proprietary Name: PSORIASIS REAL RELIEF
• Generic Name: Sulphur, Arsenicum Album, Alumen, Magnesia Sulphuricum, Natrum Sulphuricum
• Dosage Form: Tablet, Chewable
• Route of Administration: ORAL
• Marketing Start Date: 2012-07-11
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: HOMEOLAB USA INC
• Substance Name: SULFUR; ARSENIC TRIOXIDE; POTASSIUM ALUM; MAGNESIUM SULFATE HEPTAHYDRATE; SODIUM SULFATE
• Active Ingredient Strength: 8 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1
• NDC Exclude Flag: E
• Listing Certified Through: 2018-12-31

Packaging

NDC 60512-6010-0

90 TABLET, CHEWABLE in 1 BOTTLE (60512-6010-0)

• Marketing Start Date: 2012-07-11
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 60512-6010-0 [60512601000]

PSORIASIS REAL RELIEF TABLET, CHEWABLE

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2012-07-11
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
SULFUR	8 [hp_X]/1

OpenFDA Data

• SPL SET ID: 55b6982e-418a-424f-8eac-f9b61d7be436
• Manufacturer:
  • HOMEOLAB USA INC
• UNII:
  • SK47B8698T
  • 70FD1KFU70
  • 1L24V9R23S
  • S7V92P67HO
  • 0YPR65R21J
• UPC Code:
  • 0778159414602