NDC 15631-0637

MILLEFOLIUM

Millefolium

MILLEFOLIUM is a Oral Tablet 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 ID15631-0637_812f1069-6c9f-42dd-bbf3-1f735172a3c5
NDC15631-0637
Product TypeHuman Otc Drug
Proprietary NameMILLEFOLIUM
Generic NameMillefolium
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2015-12-26
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 15631-0637-0

1 TABLET in 1 BLISTER PACK (15631-0637-0)
Marketing Start Date2015-12-26
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0637-2 [15631063702]

MILLEFOLIUM TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-26
Inactivation Date2020-01-31

NDC 15631-0637-5 [15631063705]

MILLEFOLIUM TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-26
Inactivation Date2020-01-31

NDC 15631-0637-0 [15631063700]

MILLEFOLIUM TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-26
Inactivation Date2020-01-31

NDC 15631-0637-6 [15631063706]

MILLEFOLIUM TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-26
Inactivation Date2020-01-31

NDC 15631-0637-4 [15631063704]

MILLEFOLIUM TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-26
Inactivation Date2020-01-31

NDC 15631-0637-1 [15631063701]

MILLEFOLIUM TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-26
Inactivation Date2020-01-31

NDC 15631-0637-7 [15631063707]

MILLEFOLIUM TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-26
Inactivation Date2020-01-31

NDC 15631-0637-3 [15631063703]

MILLEFOLIUM TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-26
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
ACHILLEA MILLEFOLIUM1 [hp_X]/1

OpenFDA Data

SPL SET ID:1b63d304-fc28-43a5-b0b1-1f7de79a22c4
Manufacturer
UNII
UPC Code
  • 8907460005526
  • 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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