NDC 69152-1007

Sarsaparilla 30C

Sarsaparilla

Sarsaparilla 30C is a Oral Pellet in the Human Otc Drug category. It is labeled and distributed by Paramesh Banerji Life Sciences Llc. The primary component is Smilax Regelii Root.

Product ID69152-1007_30835b72-6cb9-32e8-e054-00144ff8d46c
NDC69152-1007
Product TypeHuman Otc Drug
Proprietary NameSarsaparilla 30C
Generic NameSarsaparilla
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-05-11
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameParamesh Banerji Life Sciences LLC
Substance NameSMILAX REGELII ROOT
Active Ingredient Strength30 [hp_C]/1
NDC Exclude FlagE
Listing Certified Through2017-12-31

Packaging

NDC 69152-1007-1

96 PELLET in 1 BOTTLE (69152-1007-1)
Marketing Start Date2015-05-11
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 69152-1007-1 [69152100701]

Sarsaparilla 30C PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-05-11
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
SMILAX REGELII ROOT30 [hp_C]/1

OpenFDA Data

SPL SET ID:15ce921e-d984-5f50-e054-00144ff8d46c
Manufacturer

NDC Crossover Matching brand name "Sarsaparilla 30C" or generic name "Sarsaparilla"

NDCBrand NameGeneric Name
69152-1007Sarsaparilla 30CSarsaparilla
15631-0393SARSAPARILLASARSAPARILLA
15631-0680SARSAPARILLASARSAPARILLA
37662-2148SarsaparillaSarsaparilla
37662-2149SarsaparillaSarsaparilla
37662-2150SarsaparillaSarsaparilla
37662-2151SarsaparillaSarsaparilla
37662-2152SarsaparillaSarsaparilla
37662-2153SarsaparillaSarsaparilla
37662-2154SarsaparillaSarsaparilla
37662-2155SarsaparillaSarsaparilla
37662-2156SarsaparillaSarsaparilla
62106-8848SARSAPARILLASarsaparilla
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.