NDC 15631-0077

BELLIS PERENNIS

Bellis Perennis

BELLIS PERENNIS 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 Bellis Perennis.

Product ID15631-0077_008b7aaf-da22-4736-95df-5738396f4ceb
NDC15631-0077
Product TypeHuman Otc Drug
Proprietary NameBELLIS PERENNIS
Generic NameBellis Perennis
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-09-12
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 15631-0077-0

100 PELLET in 1 PACKAGE (15631-0077-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0077-3 [15631007703]

BELLIS PERENNIS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-18

NDC 15631-0077-2 [15631007702]

BELLIS PERENNIS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-18

NDC 15631-0077-1 [15631007701]

BELLIS PERENNIS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-18

NDC 15631-0077-5 [15631007705]

BELLIS PERENNIS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-18

NDC 15631-0077-0 [15631007700]

BELLIS PERENNIS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-18

NDC 15631-0077-4 [15631007704]

BELLIS PERENNIS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-18

Drug Details

Active Ingredients

IngredientStrength
BELLIS PERENNIS1 [hp_X]/1

OpenFDA Data

SPL SET ID:157ee323-d7f2-41f4-a941-580632487359
Manufacturer
UNII

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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