NDC 63545-676

Oleum santali

Oleum Santali

Oleum santali is a Buccal; Oral; Sublingual Pellet in the Human Otc Drug category. It is labeled and distributed by Hahnemann Laboratories, Inc.. The primary component is Sandalwood Oil.

• Product ID: 63545-676_4ce57287-184e-4b5b-e054-00144ff8d46c
• NDC: 63545-676
• Product Type: Human Otc Drug
• Proprietary Name: Oleum santali
• Generic Name: Oleum Santali
• Dosage Form: Pellet
• Route of Administration: BUCCAL; ORAL; SUBLINGUAL
• Marketing Start Date: 2017-04-11
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Hahnemann Laboratories, Inc.
• Substance Name: SANDALWOOD OIL
• Active Ingredient Strength: 30 [hp_C]/[hp_C]
• NDC Exclude Flag: E
• Listing Certified Through: 2018-12-31

Packaging

NDC 63545-676-01

240 [hp_C] in 1 VIAL, GLASS (63545-676-01)

• Marketing Start Date: 2017-04-11
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 63545-676-01 [63545067601]

Oleum santali PELLET

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2017-04-11
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
SANDALWOOD OIL	30 [hp_C]/[hp_C]

OpenFDA Data

• SPL SET ID: 4ce57287-184d-4b5b-e054-00144ff8d46c
• Manufacturer:
  • Hahnemann Laboratories, Inc.
• UNII:
  • X7X01WMQ5F