NDC 60512-8035

DIAMITE

Calcarea Fluorica, Calcarea Phosphorica, Calcarea Sulphurica, Ferrum Phosphoricum, Kali Muriaticum, Kali Phosphoricum, Kali Sulphuricum, Magnesia Phosphorica, Natrum Muriaticum, Natrum Phosphoricum, Natrum Sulphuricum, Silicea

DIAMITE is a Oral Tablet, Chewable in the Human Otc Drug category. It is labeled and distributed by Homeolab Usa Inc. The primary component is Calcium Fluoride; Calcium Phosphate; Calcium Sulfate; Ferrum Phosphoricum; Potassium Chloride; Potassium Phosphate, Dibasic; Potassium Sulfate; Magnesium Phosphate, Dibasic; Sodium Chloride; Sodium Phosphate, Dibasic; Sodium Sulfate; Silicon Dioxide.

Product ID60512-8035_336b7627-d812-449a-883b-a59c92992a0b
NDC60512-8035
Product TypeHuman Otc Drug
Proprietary NameDIAMITE
Generic NameCalcarea Fluorica, Calcarea Phosphorica, Calcarea Sulphurica, Ferrum Phosphoricum, Kali Muriaticum, Kali Phosphoricum, Kali Sulphuricum, Magnesia Phosphorica, Natrum Muriaticum, Natrum Phosphoricum, Natrum Sulphuricum, Silicea
Dosage FormTablet, Chewable
Route of AdministrationORAL
Marketing Start Date2014-03-28
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameHOMEOLAB USA INC
Substance NameCALCIUM FLUORIDE; CALCIUM PHOSPHATE; CALCIUM SULFATE; FERRUM PHOSPHORICUM; POTASSIUM CHLORIDE; POTASSIUM PHOSPHATE, DIBASIC; POTASSIUM SULFATE; MAGNESIUM PHOSPHATE, DIBASIC; SODIUM CHLORIDE; SODIUM PHOSPHATE, DIBASIC; SODIUM SULFATE; SILICON DIOXIDE
Active Ingredient Strength6 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 60512-8035-5

125 TABLET, CHEWABLE in 1 JAR (60512-8035-5)
Marketing Start Date2014-03-28
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 60512-8035-5 [60512803505]

DIAMITE TABLET, CHEWABLE
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2014-03-28
Inactivation Date2020-01-31

NDC 60512-8035-6 [60512803506]

DIAMITE TABLET, CHEWABLE
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2014-03-28
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
CALCIUM FLUORIDE6 [hp_X]/1

OpenFDA Data

SPL SET ID:925223c6-b95e-4fa4-9455-f10bb02c3341
Manufacturer
UNII

NDC Crossover Matching brand name "DIAMITE" or generic name "Calcarea Fluorica, Calcarea Phosphorica, Calcarea Sulphurica, Ferrum Phosphoricum, Kali Muriaticum, Kali Phosphoricum, Kali Sulphuricum, Magnesia Phosphorica, Natrum Muriaticum, Natrum Phosphoricum, Natrum Sulphuricum, Silicea"

NDCBrand NameGeneric Name
60512-8035DIAMITECALCAREA FLUORICA, CALCAREA PHOSPHORICA, CALCAREA SULPHURICA, FERRUM PHOSPHORICUM, KALI MURIATICUM, KALI PHOSPHORICUM, KALI SULPHURICUM, MAGNESIA PHOSPHORICA, NATRUM MURIATICUM, NATRUM PHOSPHORICUM, NATRUM SULPHURICUM, SILICEA
60512-8036DIAMITECALCAREA FLUORICA, CALCAREA PHOSPHORICA, CALCAREA SULPHURICA, FERRUM PHOSPHORICUM, KALI MURIATICUM, KALI PHOSPHORICUM, KALI SULPHURICUM, MAGNESIA PHOSPHORICA, NATRUM MURIATICUM, NATRUM PHOSPHORICUM, NATRUM SULPHURICUM, SILICEA
60512-8037DIAMITE 12CALCAREA FLUORICA, CALCAREA PHOSPHORICA, CALCAREA SULPHURICA, FERRUM PHOSPHORICUM, KALI MURIATICUM, KALI PHOSPHORICUM, KALI SULPHURICUM, MAGNESIA PHOSPHORICA, NATRUM MURIATICUM, NATRUM PHOSPHORICUM, NATRUM SULPHURICUM, SILICEA

Trademark Results [DIAMITE]

Mark Image

Registration | Serial
Company
Trademark
Application Date
DIAMITE
DIAMITE
74195736 1698961 Dead/Cancelled
Diamite Corporation
1991-08-19
DIAMITE
DIAMITE
73661836 1471932 Dead/Cancelled
DIAMITE CORPORATION
1987-05-20
DIAMITE
DIAMITE
73616572 1438907 Live/Registered
DIAMITE CORPORATION
1986-08-25
DIAMITE
DIAMITE
73063203 1053261 Dead/Cancelled
Ottaviani; Peter
1975-09-16
DIAMITE
DIAMITE
72179491 0773498 Dead/Cancelled
WEATHERLY FOUNDRY AND MANUFACTURINGCOMPANY
1963-10-21

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