NDC 63545-691

Zincum Oxydatum

Zincum Oxydatum

Zincum Oxydatum 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 Zinc Oxide.

• Product ID: 63545-691_4f072bb7-d5d5-68b3-e054-00144ff88e88
• NDC: 63545-691
• Product Type: Human Otc Drug
• Proprietary Name: Zincum Oxydatum
• Generic Name: Zincum Oxydatum
• Dosage Form: Pellet
• Route of Administration: BUCCAL; ORAL; SUBLINGUAL
• Marketing Start Date: 2017-05-08
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Hahnemann Laboratories, Inc.
• Substance Name: ZINC OXIDE
• Active Ingredient Strength: 30 [hp_C]/[hp_C]
• NDC Exclude Flag: E
• Listing Certified Through: 2018-12-31

Packaging

NDC 63545-691-01

240 [hp_C] in 1 VIAL, GLASS (63545-691-01)

• Marketing Start Date: 2017-05-08
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 63545-691-01 [63545069101]

Zincum Oxydatum PELLET

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2017-05-08
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
ZINC OXIDE	30 [hp_C]/[hp_C]

OpenFDA Data

• SPL SET ID: 4f072bb7-d5d4-68b3-e054-00144ff88e88
• Manufacturer:
  • Hahnemann Laboratories, Inc.
• UNII:
  • SOI2LOH54Z

NDC Crossover Matching brand name "Zincum Oxydatum" or generic name "Zincum Oxydatum"

NDC	Brand Name	Generic Name
37662-1969	Zincum Oxydatum	Zincum Oxydatum
37662-1970	Zincum Oxydatum	Zincum Oxydatum
37662-1971	Zincum Oxydatum	Zincum Oxydatum
37662-1972	Zincum Oxydatum	Zincum Oxydatum
37662-1973	Zincum Oxydatum	Zincum Oxydatum
37662-1974	Zincum Oxydatum	Zincum Oxydatum
37662-1975	Zincum Oxydatum	Zincum Oxydatum
37662-1976	Zincum Oxydatum	Zincum Oxydatum
63545-691	Zincum Oxydatum	Zincum Oxydatum
71919-729	ZINCUM OXYDATUM	ZINC OXIDE