NDC 0220-2946

Kreosotum

Wood Creosote

Kreosotum is a Oral Pellet in the Human Otc Drug category. It is labeled and distributed by Laboratoires Boiron. The primary component is Wood Creosote.

• Product ID: 0220-2946_5fd8d14c-c2c0-de71-e053-2991aa0a7225
• NDC: 0220-2946
• Product Type: Human Otc Drug
• Proprietary Name: Kreosotum
• Generic Name: Wood Creosote
• Dosage Form: Pellet
• Route of Administration: ORAL
• Marketing Start Date: 1983-03-03
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Laboratoires Boiron
• Substance Name: WOOD CREOSOTE
• Active Ingredient Strength: 12 [hp_C]/1
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 0220-2946-41

80 PELLET in 1 TUBE (0220-2946-41)

• Marketing Start Date: 1983-03-03
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 0220-2946-41 [00220294641]

Kreosotum PELLET

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 1983-03-03

Drug Details

Active Ingredients

Ingredient	Strength
WOOD CREOSOTE	12 [hp_C]/1

OpenFDA Data

• SPL SET ID: 19fe8720-7c5e-11e6-85cf-424c58303031
• Manufacturer:
  • Laboratoires Boiron
• UNII:
  • 3JYG22FD73

NDC Crossover Matching brand name "Kreosotum" or generic name "Wood Creosote"

NDC	Brand Name	Generic Name
0220-2940	Kreosotum	WOOD CREOSOTE
0220-2943	Kreosotum	WOOD CREOSOTE
0220-2944	Kreosotum	WOOD CREOSOTE
0220-2946	Kreosotum	WOOD CREOSOTE
15631-0256	KREOSOTUM	KREOSOTUM
15631-0615	KREOSOTUM	KREOSOTUM
68428-461	Kreosotum	WOOD CREOSOTE
71919-394	Kreosotum	WOOD CREOSOTE
64117-248	INCONTINENCE VOMITING	WOOD CREOSOTE
69152-1048	Kreosotum 200C	Kreosotum