NDC 48951-8029

Phosphorus comp.

Phosphorus Comp.

Phosphorus comp. is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Uriel Pharmacy Inc.. The primary component is Cupric Sulfate; Sus Scrofa Pancreas; Phosphorus; Rosmarinus Officinalis Flowering Top; Amber; Silicon Dioxide; Silver.

• Product ID: 48951-8029_6d088ab6-ce97-58ab-e053-2a91aa0aafb6
• NDC: 48951-8029
• Product Type: Human Otc Drug
• Proprietary Name: Phosphorus comp.
• Generic Name: Phosphorus Comp.
• Dosage Form: Liquid
• Route of Administration: ORAL
• Marketing Start Date: 2009-09-01
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Uriel Pharmacy Inc.
• Substance Name: CUPRIC SULFATE; SUS SCROFA PANCREAS; PHOSPHORUS; ROSMARINUS OFFICINALIS FLOWERING TOP; AMBER; SILICON DIOXIDE; SILVER
• Active Ingredient Strength: 4 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 48951-8029-1

10 AMPULE in 1 BOX (48951-8029-1) > 1 mL in 1 AMPULE

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

NDC SPL Data Element Entries

NDC 48951-8029-1 [48951802901]

Phosphorus comp. LIQUID

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

Drug Details

Active Ingredients

Ingredient	Strength
CUPRIC SULFATE	4 [hp_X]/mL

OpenFDA Data

• SPL SET ID: 0fb3b1ca-f964-41c3-b9e7-c4f3b5fc5e8e
• Manufacturer:
  • Uriel Pharmacy Inc.
• UNII:
  • ETJ7Z6XBU4
  • 8JM482TI79
  • 3M4G523W1G
  • 70J9Z0J26P
  • 27YLU75U4W
  • 9Y3J3362RY
  • LRX7AJ16DT

NDC Crossover Matching brand name "Phosphorus comp." or generic name "Phosphorus Comp."

NDC	Brand Name	Generic Name
48951-8029	Phosphorus comp.	Phosphorus comp.
48951-8030	Phosphorus comp.	Phosphorus comp.