NDC 69152-1048

Kreosotum 200C

Kreosotum

Kreosotum 200C is a Oral Pellet in the Human Otc Drug category. It is labeled and distributed by Paramesh Banerji Life Sciences Llc. The primary component is Wood Creosote.

• Product ID: 69152-1048_2f2dc04a-4e0c-1409-e054-00144ff88e88
• NDC: 69152-1048
• Product Type: Human Otc Drug
• Proprietary Name: Kreosotum 200C
• Generic Name: Kreosotum
• Dosage Form: Pellet
• Route of Administration: ORAL
• Marketing Start Date: 2015-06-20
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Paramesh Banerji Life Sciences LLC
• Substance Name: WOOD CREOSOTE
• Active Ingredient Strength: 200 [hp_C]/1
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 69152-1048-1

96 PELLET in 1 BOTTLE (69152-1048-1)

• Marketing Start Date: 2015-06-20
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 69152-1048-1 [69152104801]

Kreosotum 200C PELLET

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2015-06-20
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
WOOD CREOSOTE	200 [hp_C]/1

OpenFDA Data

• SPL SET ID: 18ee7dbe-7f0c-4d13-e054-00144ff8d46c
• Manufacturer:
  • Paramesh Banerji Life Sciences LLC
• UNII:
  • 3JYG22FD73

NDC Crossover Matching brand name "Kreosotum 200C" or generic name "Kreosotum"

NDC	Brand Name	Generic Name
69152-1048	Kreosotum 200C	Kreosotum
15631-0256	KREOSOTUM	KREOSOTUM
15631-0615	KREOSOTUM	KREOSOTUM