NDC 69152-1198

Sulphur 200C

Sulphur

Sulphur 200C 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 Sulfur.

Product ID69152-1198_36693891-e340-24c3-e054-00144ff8d46c
NDC69152-1198
Product TypeHuman Otc Drug
Proprietary NameSulphur 200C
Generic NameSulphur
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-06-30
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameParamesh Banerji Life Sciences LLC
Substance NameSULFUR
Active Ingredient Strength200 [hp_C]/1
NDC Exclude FlagE
Listing Certified Through2017-12-31

Packaging

NDC 69152-1198-1

96 PELLET in 1 BOTTLE (69152-1198-1)
Marketing Start Date2015-06-30
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 69152-1198-1 [69152119801]

Sulphur 200C PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-06-30
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
SULFUR200 [hp_C]/1

OpenFDA Data

SPL SET ID:19b8ecbe-bfbc-72db-e054-00144ff88e88
Manufacturer
UNII

NDC Crossover Matching brand name "Sulphur 200C" or generic name "Sulphur"

NDCBrand NameGeneric Name
69152-1198Sulphur 200CSulphur
72827-100Matys Organic Baby Eczema ReliefSulphur
0295-7300ProsaceaSulphur
52389-173ProsaceaSulphur
0360-0369SULPHURSULPHUR
15631-0420SULPHURSULPHUR
15631-0692SULPHURSULPHUR
15631-2322SULPHURSULPHUR
37662-2313SulphurSulphur
37662-2314SulphurSulphur
37662-2315SulphurSulphur
37662-2316SulphurSulphur
37662-2317SulphurSulphur
37662-2318SulphurSulphur
37662-2319SulphurSulphur
37662-2320SulphurSulphur
37662-2321SulphurSulphur
44911-0394SulphurSulphur
55714-6516SulphurSulphur
55714-7516SulphurSulphur
60512-1047SULPHURSULPHUR
63083-7138SulphurSulphur
76472-3037SULPHURSULPHUR
43406-0472Sulphur 30CSulphur
51439-004Treatment 101Sulphur
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