NDC 62106-8812

SABAL SERRULATA

Saw Palmetto

SABAL SERRULATA is a Oral Granule in the Human Otc Drug category. It is labeled and distributed by Seroyal Usa. The primary component is Saw Palmetto.

Product ID62106-8812_1bdf0063-0486-4017-e054-00144ff8d46c
NDC62106-8812
Product TypeHuman Otc Drug
Proprietary NameSABAL SERRULATA
Generic NameSaw Palmetto
Dosage FormGranule
Route of AdministrationORAL
Marketing Start Date2015-07-27
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameSeroyal USA
Substance NameSAW PALMETTO
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 62106-8812-4

10 TUBE in 1 CARTON (62106-8812-4) > 140 GRANULE in 1 TUBE
Marketing Start Date2015-07-27
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 62106-8812-4 [62106881204]

SABAL SERRULATA GRANULE
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-07-27

Drug Details

Active Ingredients

IngredientStrength
SAW PALMETTO1 [hp_X]/1

OpenFDA Data

SPL SET ID:1bdf0063-0485-4017-e054-00144ff8d46c
Manufacturer
UNII

NDC Crossover Matching brand name "SABAL SERRULATA" or generic name "Saw Palmetto"

NDCBrand NameGeneric Name
0220-4503Sabal serrulataSAW PALMETTO
0220-4507Sabal serrulataSAW PALMETTO
0220-4508Sabal serrulataSAW PALMETTO
0360-0336SABAL SERRULATASABAL SERR
15631-0381SABAL SERRULATASABAL SERRULATA
15631-0675SABAL SERRULATASABAL SERRULATA
37662-1200Sabal SerrulataSabal Serrulata
37662-1201Sabal SerrulataSabal Serrulata
37662-1202Sabal SerrulataSabal Serrulata
37662-1203Sabal SerrulataSabal Serrulata
37662-1204Sabal SerrulataSabal Serrulata
37662-1205Sabal SerrulataSabal Serrulata
37662-1206Sabal SerrulataSabal Serrulata
62106-8812SABAL SERRULATASaw palmetto
71919-597Sabal serrulataSAW PALMETTO
64117-177Painful UrinationSAW PALMETTO
68428-611SabalSAW PALMETTO
0220-4506Sabal serrualataSAW PALMETTO
69152-1556Sabal serrulata 1XSabal serrulata

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.