NDC 15631-0297

MILLEFOLIUM

Millefolium

MILLEFOLIUM is a Oral Pellet in the Human Otc Drug category. It is labeled and distributed by Rxhomeo Private Limited D.b.a. Rxhomeo, Inc. The primary component is Achillea Millefolium.

Product ID15631-0297_0785ca18-5d0f-4fa1-98e4-110b902dc0b7
NDC15631-0297
Product TypeHuman Otc Drug
Proprietary NameMILLEFOLIUM
Generic NameMillefolium
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-09-10
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameACHILLEA MILLEFOLIUM
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0297-0

100 PELLET in 1 PACKAGE (15631-0297-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0297-1 [15631029701]

MILLEFOLIUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-24

NDC 15631-0297-0 [15631029700]

MILLEFOLIUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-24

NDC 15631-0297-5 [15631029705]

MILLEFOLIUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-24

NDC 15631-0297-4 [15631029704]

MILLEFOLIUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-24

NDC 15631-0297-3 [15631029703]

MILLEFOLIUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-24

NDC 15631-0297-2 [15631029702]

MILLEFOLIUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-24

Drug Details

Active Ingredients

IngredientStrength
ACHILLEA MILLEFOLIUM1 [hp_X]/1

OpenFDA Data

SPL SET ID:6ca2dfa5-64c5-40e9-9d39-ea581fa86d7b
Manufacturer
UNII

NDC Crossover Matching brand name "MILLEFOLIUM" or generic name "Millefolium"

NDCBrand NameGeneric Name
0220-3445MillefoliumACHILLEA MILLEFOLIUM
0220-3462MillefoliumACHILLEA MILLEFOLIUM
0220-3463MillefoliumACHILLEA MILLEFOLIUM
15631-0297MILLEFOLIUMMILLEFOLIUM
15631-0637MILLEFOLIUMMILLEFOLIUM
53645-1330MillefoliumMillefolium
68428-512MillefoliumACHILLEA MILLEFOLIUM
71919-466MillefoliumACHILLEA MILLEFOLIUM
69152-1202Millefolium 6CMillefolium

Trademark Results [MILLEFOLIUM]

Mark Image

Registration | Serial
Company
Trademark
Application Date
MILLEFOLIUM
MILLEFOLIUM
76409805 2720969 Live/Registered
Millefolium International Inc.
2002-05-08

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