NDC 15631-0618

LAC FELINUM

Lac Felinum

LAC FELINUM 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 Felis Catus Milk.

Product ID15631-0618_1df7feb9-f828-4fba-90d1-9b25facb6978
NDC15631-0618
Product TypeHuman Otc Drug
Proprietary NameLAC FELINUM
Generic NameLac Felinum
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2015-12-21
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameFELIS CATUS MILK
Active Ingredient Strength3 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0618-6

1000 TABLET in 1 CONTAINER (15631-0618-6)
Marketing Start Date2015-12-21
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0618-1 [15631061801]

LAC FELINUM TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-21
Inactivation Date2020-01-31

NDC 15631-0618-6 [15631061806]

LAC FELINUM TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-21
Inactivation Date2020-01-31

NDC 15631-0618-3 [15631061803]

LAC FELINUM TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-21
Inactivation Date2020-01-31

NDC 15631-0618-7 [15631061807]

LAC FELINUM TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-21
Inactivation Date2020-01-31

NDC 15631-0618-2 [15631061802]

LAC FELINUM TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-21
Inactivation Date2020-01-31

NDC 15631-0618-4 [15631061804]

LAC FELINUM TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-21
Inactivation Date2020-01-31

NDC 15631-0618-5 [15631061805]

LAC FELINUM TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-21
Inactivation Date2020-01-31

NDC 15631-0618-0 [15631061800]

LAC FELINUM TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-21
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
FELIS CATUS MILK3 [hp_X]/1

OpenFDA Data

SPL SET ID:21d8816a-4e81-43a1-9e58-493e2af36f0e
Manufacturer
UNII
UPC Code
  • 8907460005526
  • NDC Crossover Matching brand name "LAC FELINUM" or generic name "Lac Felinum"

    NDCBrand NameGeneric Name
    15631-0259LAC FELINUMLAC FELINUM
    15631-0618LAC FELINUMLAC FELINUM
    68428-969Lac felinumFELIS CATUS MILK
    71919-398Lac felinumFELIS CATUS MILK

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