- Product NDC
- 60512-8037
- 11-digit product format
- 605128037
- Labeler code
- 60512
- Product ID
- 60512-8037_e21074b8-af22-4a03-8b6b-c2d1aa0f6e21
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- CALCAREA FLUORICA, CALCAREA PHOSPHORICA, CALCAREA SULPHURICA, FERRUM PHOSPHORICUM, KALI MURIATICUM, KALI PHOSPHORICUM, KALI SULPHURICUM, MAGNESIA PHOSPHORICA, NATRUM MURIATICUM, NATRUM PHOSPHORICUM, NATRUM SULPHURICUM, SILICEA
- Dosage form
- TABLET, CHEWABLE
- Route
- ORAL
- Labeler
- HOMEOLAB USA INC
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2015-06-12
- Marketing end
- 0000-00-00
- Substance
- 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
- Active strength
- 6 [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 flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record