NDC 60512-6030

ALLERGY REAL RELIEF

Allium Cepa, Arsenicum Album, Nux Vomica, Euphrasia Officinalis, Sabadilla, Sticta Pulmonaria, Aralia Racemosa, Cuprum Metallicum

ALLERGY REAL RELIEF is a Oral Tablet, Chewable in the Human Otc Drug category. It is labeled and distributed by Homeolab Usa Inc.. The primary component is Onion; Arsenic Trioxide; Strychnos Nux-vomica Seed; Euphrasia Stricta; Schoenocaulon Officinale Seed; Lobaria Pulmonaria; Aralia Racemosa Root; Copper.

• Product ID: 60512-6030_1ea40849-40eb-4be7-b343-52f1fd5dc57c
• NDC: 60512-6030
• Product Type: Human Otc Drug
• Proprietary Name: ALLERGY REAL RELIEF
• Generic Name: Allium Cepa, Arsenicum Album, Nux Vomica, Euphrasia Officinalis, Sabadilla, Sticta Pulmonaria, Aralia Racemosa, Cuprum Metallicum
• Dosage Form: Tablet, Chewable
• Route of Administration: ORAL
• Marketing Start Date: 2012-10-25
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: HOMEOLAB USA INC.
• Substance Name: ONION; ARSENIC TRIOXIDE; STRYCHNOS NUX-VOMICA SEED; EUPHRASIA STRICTA; SCHOENOCAULON OFFICINALE SEED; LOBARIA PULMONARIA; ARALIA RACEMOSA ROOT; COPPER
• Active Ingredient Strength: 8 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1
• NDC Exclude Flag: E
• Listing Certified Through: 2018-12-31

Packaging

NDC 60512-6030-0

90 TABLET, CHEWABLE in 1 BOTTLE (60512-6030-0)

• Marketing Start Date: 2012-10-25
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 60512-6030-0 [60512603000]

ALLERGY REAL RELIEF TABLET, CHEWABLE

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2012-10-25
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
ONION	8 [hp_X]/1

OpenFDA Data

• SPL SET ID: 10f0b41c-1477-42b7-b35c-839283f5918a
• Manufacturer:
  • HOMEOLAB USA INC.
• UNII:
  • D1YM0P5Z2T
  • 6NAF1689IO
  • S7V92P67HO
  • 789U1901C5
  • C9642I91WL
  • T90W4582DU
  • 269XH13919
  • 492225Q21H