NDC 15631-0537

BELLIS PERENNIS

Bellis Perennis

BELLIS PERENNIS 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 Bellis Perennis.

Product ID15631-0537_df16336a-d3a8-4f3a-9a67-166d79bbed0e
NDC15631-0537
Product TypeHuman Otc Drug
Proprietary NameBELLIS PERENNIS
Generic NameBellis Perennis
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2015-12-30
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameBELLIS PERENNIS
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0537-0

1 TABLET in 1 BLISTER PACK (15631-0537-0)
Marketing Start Date2015-12-30
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0537-7 [15631053707]

BELLIS PERENNIS TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-30
Inactivation Date2020-01-31

NDC 15631-0537-4 [15631053704]

BELLIS PERENNIS TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-30
Inactivation Date2020-01-31

NDC 15631-0537-1 [15631053701]

BELLIS PERENNIS TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-30
Inactivation Date2020-01-31

NDC 15631-0537-0 [15631053700]

BELLIS PERENNIS TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-30
Inactivation Date2020-01-31

NDC 15631-0537-5 [15631053705]

BELLIS PERENNIS TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-30
Inactivation Date2020-01-31

NDC 15631-0537-2 [15631053702]

BELLIS PERENNIS TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-30
Inactivation Date2020-01-31

NDC 15631-0537-6 [15631053706]

BELLIS PERENNIS TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-30
Inactivation Date2020-01-31

NDC 15631-0537-3 [15631053703]

BELLIS PERENNIS TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-30
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
BELLIS PERENNIS1 [hp_X]/1

OpenFDA Data

SPL SET ID:d14ee0c6-b6a8-4f2b-ac72-c09065d649ec
Manufacturer
UNII
UPC Code
  • 8907460005526
  • NDC Crossover Matching brand name "BELLIS PERENNIS" or generic name "Bellis Perennis"

    NDCBrand NameGeneric Name
    0220-0731Bellis perennisBELLIS PERENNIS
    0220-0732Bellis perennisBELLIS PERENNIS
    0220-0733Bellis perennisBELLIS PERENNIS
    0220-0734Bellis perennisBELLIS PERENNIS
    0220-0811Bellis perennisBELLIS PERENNIS
    0220-0812Bellis perennisBELLIS PERENNIS
    0220-0816Bellis perennisBELLIS PERENNIS
    15631-0077BELLIS PERENNISBELLIS PERENNIS
    15631-0537BELLIS PERENNISBELLIS PERENNIS
    60512-6541BELLIS PERENNISBELLIS PERENNIS
    62106-7479BELLIS PERENNISDaisy
    63545-420Bellis PerennisBellis Perennis
    63545-421Bellis PerennisBellis Perennis
    63545-422Bellis PerennisBellis Perennis
    63545-423Bellis PerennisBellis Perennis
    63545-424Bellis PerennisBellis Perennis
    63545-425Bellis PerennisBellis Perennis
    63545-426Bellis PerennisBellis Perennis
    63545-427Bellis PerennisBellis Perennis
    66096-798Bellis PerennisBELLIS PERENNIS
    68428-252Bellis perennisBELLIS PERENNIS
    79718-1081Bellis PerennisBellis Perennis
    71919-115BELLISBELLIS PERENNIS
    68428-133Bellis Perennis Kit RefillBELLIS PERENNIS
    71919-773Bellis Perennis Kit RefillBELLIS PERENNIS
    64117-960Sprains BruisesBELLIS PERENNIS

    Trademark Results [BELLIS PERENNIS]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    BELLIS PERENNIS
    BELLIS PERENNIS
    97388344 not registered Live/Pending
    Di Martino, Natalia
    2022-04-29

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