NDC 15631-0255

KALMIA LATIFOLIA

Kalmia Latifolia

KALMIA LATIFOLIA 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 Kalmia Latifolia Leaf.

Product ID15631-0255_9b3035da-170a-4a37-8b32-b09e23a0881b
NDC15631-0255
Product TypeHuman Otc Drug
Proprietary NameKALMIA LATIFOLIA
Generic NameKalmia Latifolia
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-09-05
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameKALMIA LATIFOLIA LEAF
Active Ingredient Strength3 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0255-0

100 PELLET in 1 PACKAGE (15631-0255-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0255-2 [15631025502]

KALMIA LATIFOLIA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-23

NDC 15631-0255-0 [15631025500]

KALMIA LATIFOLIA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-23

NDC 15631-0255-4 [15631025504]

KALMIA LATIFOLIA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-23

NDC 15631-0255-5 [15631025505]

KALMIA LATIFOLIA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-23

NDC 15631-0255-1 [15631025501]

KALMIA LATIFOLIA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-23

NDC 15631-0255-3 [15631025503]

KALMIA LATIFOLIA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-23

Drug Details

Active Ingredients

IngredientStrength
KALMIA LATIFOLIA LEAF3 [hp_X]/1

OpenFDA Data

SPL SET ID:91042d4d-dc32-4a02-8203-fda0f5ef1c15
Manufacturer
UNII

NDC Crossover Matching brand name "KALMIA LATIFOLIA" or generic name "Kalmia Latifolia"

NDCBrand NameGeneric Name
0220-2927Kalmia latifoliaKALMIA LATIFOLIA LEAF
0220-2928Kalmia latifoliaKALMIA LATIFOLIA LEAF
0220-2931Kalmia latifoliaKALMIA LATIFOLIA LEAF
0220-2932Kalmia latifoliaKALMIA LATIFOLIA LEAF
0220-2934Kalmia latifoliaKALMIA LATIFOLIA LEAF
15631-0255KALMIA LATIFOLIAKALMIA LATIFOLIA
62106-8250KALMIA LATIFOLIAMountain laurel
68428-458Kalmia latifoliaKALMIA LATIFOLIA LEAF
71919-390Kalmia latifoliaKALMIA LATIFOLIA LEAF

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