NDC 60512-6479

AMBROSIA ARTEMISIAEFOLIA

Ambrosia Artemisiaefolia

AMBROSIA ARTEMISIAEFOLIA is a Oral Pellet in the Human Otc Drug category. It is labeled and distributed by Homeolab Usa Inc.. The primary component is Ambrosia Artemisiifolia.

• Product ID: 60512-6479_3f54f17f-a819-4667-bbb9-df8ab29aae80
• NDC: 60512-6479
• Product Type: Human Otc Drug
• Proprietary Name: AMBROSIA ARTEMISIAEFOLIA
• Generic Name: Ambrosia Artemisiaefolia
• Dosage Form: Pellet
• Route of Administration: ORAL
• Marketing Start Date: 1995-10-11
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: HOMEOLAB USA INC.
• Substance Name: AMBROSIA ARTEMISIIFOLIA
• Active Ingredient Strength: 1 [hp_X]/1
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 60512-6479-1

80 PELLET in 1 TUBE (60512-6479-1)

• Marketing Start Date: 1995-10-11
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 60512-6479-1 [60512647901]

AMBROSIA ARTEMISIAEFOLIA PELLET

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 1995-10-11
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
AMBROSIA ARTEMISIIFOLIA	1 [hp_X]/1

OpenFDA Data

• SPL SET ID: 5effb2f5-f892-4255-b394-9d7aac4b883e
• Manufacturer:
  • HOMEOLAB USA INC.
• UNII:
  • 9W34L2CQ9A

NDC Crossover Matching brand name "AMBROSIA ARTEMISIAEFOLIA" or generic name "Ambrosia Artemisiaefolia"

NDC	Brand Name	Generic Name
0220-0218	Ambrosia artemisiaefolia	AMBROSIA ARTEMISIIFOLIA
0220-0219	Ambrosia artemisiaefolia	AMBROSIA ARTEMISIIFOLIA
0220-0225	Ambrosia artemisiaefolia	AMBROSIA ARTEMISIIFOLIA
15631-0024	AMBROSIA ARTEMISIAEFOLIA	AMBROSIA ARTEMISIAEFOLIA
60512-6479	AMBROSIA ARTEMISIAEFOLIA	AMBROSIA ARTEMISIAEFOLIA
68428-196	Ambrosia artemisiaefolia	AMBROSIA ARTEMISIIFOLIA
71919-038	Ambrosia artemisiaefolia	AMBROSIA ARTEMISIIFOLIA
76097-003	Pollen Guard Ragweed	Ambrosia Artemisiaefolia