NDC 60512-6475

ALOE

Aloe

ALOE is a Oral Pellet in the Human Otc Drug category. It is labeled and distributed by Homeolab Usa Inc.. The primary component is Aloe Vera Leaf.

• Product ID: 60512-6475_464b4639-3bb8-4ccc-80a9-db911108be7e
• NDC: 60512-6475
• Product Type: Human Otc Drug
• Proprietary Name: ALOE
• Generic Name: Aloe
• Dosage Form: Pellet
• Route of Administration: ORAL
• Marketing Start Date: 2013-11-14
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: HOMEOLAB USA INC.
• Substance Name: ALOE VERA LEAF
• Active Ingredient Strength: 6 [hp_X]/1
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 60512-6475-1

80 PELLET in 1 TUBE (60512-6475-1)

• Marketing Start Date: 2013-11-14
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 60512-6475-1 [60512647501]

ALOE PELLET

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2013-11-14
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
ALOE VERA LEAF	6 [hp_X]/1

OpenFDA Data

• SPL SET ID: 31c2e372-f4df-4fa2-b451-1c1e246be338
• Manufacturer:
  • HOMEOLAB USA INC.
• UNII:
  • ZY81Z83H0X

NDC Crossover Matching brand name "ALOE" or generic name "Aloe"

NDC	Brand Name	Generic Name
0220-0187	Aloe	ALOE FEROX LEAF
0220-0189	Aloe	ALOE FEROX LEAF
0220-0190	Aloe	ALOE FEROX LEAF
0220-0191	Aloe	ALOE FEROX LEAF
60512-6475	ALOE	ALOE
62106-7275	ALOE	Aloe
68428-190	Aloe Socotrina	ALOE
71919-031	Aloe socotrina	ALOE
64117-504	Diarrhea	ALOE