NDC 0360-0308

PHYTOLACCA

Phytolacca

PHYTOLACCA is a Sublingual Tablet in the Human Otc Drug category. It is labeled and distributed by Standard Homeopathic Company. The primary component is Phytolacca Americana Root.

• Product ID: 0360-0308_7d406730-c332-45f2-e053-2a91aa0afb74
• NDC: 0360-0308
• Product Type: Human Otc Drug
• Proprietary Name: PHYTOLACCA
• Generic Name: Phytolacca
• Dosage Form: Tablet
• Route of Administration: SUBLINGUAL
• Marketing Start Date: 1997-02-17
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: STANDARD HOMEOPATHIC COMPANY
• Substance Name: PHYTOLACCA AMERICANA ROOT
• Active Ingredient Strength: 30 [hp_X]/g
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 0360-0308-01

1 g in 1 BOTTLE, PLASTIC (0360-0308-01)

• Marketing Start Date: 1997-02-17
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 0360-0308-01 [00360030801]

PHYTOLACCA TABLET

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 1997-02-17

Drug Details

Active Ingredients

Ingredient	Strength
PHYTOLACCA AMERICANA ROOT	30 [hp_X]/g

OpenFDA Data

• SPL SET ID: 4daf39ce-5c78-216a-e054-00144ff8d46c
• Manufacturer:
  • STANDARD HOMEOPATHIC COMPANY
• UNII:
  • 11E6VI8VEG
• UPC Code:
  • 0300360030816

NDC Crossover Matching brand name "PHYTOLACCA" or generic name "Phytolacca"

NDC	Brand Name	Generic Name
0360-0306	PHYTOLACCA	PHYTOLACCA
0360-0308	PHYTOLACCA	PHYTOLACCA
43742-0307	Phytolacca	Phytolacca Decandra