NDC 43742-0179

Sulphur Remedy

Sulphur, Asclepias Tuberosa, Bryonia, Dulcamara,

Sulphur Remedy is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Deseret Biologicals, Inc.. The primary component is Sulfur; Asclepias Tuberosa Root; Bryonia Alba Root; Solanum Dulcamara Stem.

• Product ID: 43742-0179_61bfd841-02a7-41d5-b58b-983eadf16ecf
• NDC: 43742-0179
• Product Type: Human Otc Drug
• Proprietary Name: Sulphur Remedy
• Generic Name: Sulphur, Asclepias Tuberosa, Bryonia, Dulcamara,
• Dosage Form: Liquid
• Route of Administration: ORAL
• Marketing Start Date: 2012-10-12
• Marketing End Date: 2020-09-15
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Deseret Biologicals, Inc.
• Substance Name: SULFUR; ASCLEPIAS TUBEROSA ROOT; BRYONIA ALBA ROOT; SOLANUM DULCAMARA STEM
• Active Ingredient Strength: 4 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
• NDC Exclude Flag: N

Packaging

NDC 43742-0179-1

30 mL in 1 BOTTLE, DROPPER (43742-0179-1)

• Marketing Start Date: 2012-10-12
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 43742-0179-1 [43742017901]

Sulphur Remedy LIQUID

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2012-10-12
• Marketing End Date: 2020-09-15

Drug Details

Active Ingredients

Ingredient	Strength
SULFUR	4 [hp_X]/mL

OpenFDA Data

• SPL SET ID: 9331e408-56e5-4b99-babc-9cf29f61fe91
• Manufacturer:
  • Deseret Biologicals, Inc.
• UNII:
  • 1ZL82U5D18
  • IR986LE7DF
  • 70FD1KFU70
  • T7J046YI2B

NDC Crossover Matching brand name "Sulphur Remedy" or generic name "Sulphur, Asclepias Tuberosa, Bryonia, Dulcamara,"

NDC	Brand Name	Generic Name
43742-0179	Sulphur Remedy	Sulphur, Asclepias tuberosa, Bryonia, Dulcamara,
43742-0745	Sulphur Remedy	Sulphur, Asclepias Tuberosa, Bryonia, Dulcamara