Dosage and administration
Adults and children over 12 years: dissolve 2 tablets under the tongue every 15 minutes for 2 hours before chemotherapy, then 2 tablets every 4 hours for 7 to 10 days. Children under 12 years: use half the adult dose.
DRUG FACTS:
- Manufacturer
- ZRG Detox, Inc. | Apotheca Company
- Effective date
- 2026-05-19
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 2
- Source
- full-release
- Hydrated at
- 2026-06-01 02:38:38
Label at a glance#
ProductPrequimm
Active ingredientSILVER NITRATE, COLCHICUM AUTUMNALE BULB, CONIUM MACULATUM FLOWERING TOP, IPECAC, STRYCHNOS NUX-VOMICA SEED, PULSATILLA PRATENSIS WHOLE, VERATRUM ALBUM ROOT
Label structure10 sections
Contacts and useful links#
Websitewww.zrgdetox.com
www.zrgdetox.com
www.zrgdetox.comLabel contents#
Full prescribing information#
ACTIVE INGREDIENTS:
Each 300mg tablet contains equal amounts of: Argentum Nitricum 6X, Colchicum Autumnale 4X, 6X, Conium Maculatum 4X, Ipecacuanha 4X, 30X, 200X, Nux Vomica 5X, Pulsatilla (Pratensis)6X, Veratrum Album 8X, 30X, 200X.
PURPOSE:
Temporarily relieves nausea and vomiting occurring with chemotherapy treatments.
WARNINGS:
Keep out of reach of children.
If pregnant or nursing, ask a healthcare professional before use.
Do not use if you have a known allergy to any ingredient in.
If symptoms persist or worsen, consult your doctor.
In case of overdose, get medical help or contact a Poison Control Center right away.
KEEP OUT OF REACH OF CHILDREN:
Keep out of reach of children.
DIRECTIONS:
Adults and children over 12 years:
dissolve 2 tablets under the tongue every 15 minutes for 2 hours before chemotherapy,
then 2 tablets every 4 hours for 7 to 10 days.
Children under 12 years: use half the adult dose.
OTHER INFORMATION:
Store tightly closed in a cool and dry place.
Tamper evident: Use this product only if neck seal is intact.
INDICATIONS:
Temporarily relieves nausea and vomiting occurring with chemotherapy treatments.
INACTIVE INGREDIENTS:
Lactose, Magnesium Stearate.
QUESTIONS:
PACKAGE LABEL DISPLAY:
NDC: 62630-002-17
PREQUIMM
TEMPORARILY RELIEVES NAUSEA
AND VOMITING OCCURRING WITH
CHEMOTHERAPY TREATMENTS
HOMEOPATHIC MEDICINE
100TABLETS
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| 6cca4355-1206-91f7-02de-17eef38a8622 | Product name | 1 | 20140508 |
| 751c581a-bf64-2fd7-b3ec-ca02c83e4a00 | Product name | 1 | 20140508 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 62630-002-17 | Prequimm | 100 in 1 BOTTLE | TABLET | 100 | 2 |
Products#
Every source-derived product name is available through these pages.
- Prequimm
- Argentum Nitricum, Colchicum Autumnale, Conium Maculatum, Ipecacuanha, Nux Vomica, Pulsatilla (Pratensis), Veratrum Album
- SILVER NITRATE
- SILVER CATION
- COLCHICUM AUTUMNALE BULB
- CONIUM MACULATUM FLOWERING TOP
- IPECAC
- STRYCHNOS NUX-VOMICA SEED
- PULSATILLA PRATENSIS WHOLE
- VERATRUM ALBUM ROOT
- LACTOSE MONOHYDRATE
- MAGNESIUM PALMITOSTEARATE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 62630-002 | 62630-002-17 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| SILVER NITRATE | 95IT3W8JZE | ACTIB |
| COLCHICUM AUTUMNALE BULB | 993QHL78E6 | ACTIB |
| CONIUM MACULATUM FLOWERING TOP | Q28R5GF371 | ACTIB |
| IPECAC | 62I3C8233L | ACTIB |
| STRYCHNOS NUX-VOMICA SEED | 269XH13919 | ACTIB |
| PULSATILLA PRATENSIS WHOLE | 8E272251DI | ACTIB |
| VERATRUM ALBUM ROOT | QNS6W5US1Z | ACTIB |
| LACTOSE MONOHYDRATE | EWQ57Q8I5X | IACT |
| MAGNESIUM PALMITOSTEARATE | R4OXA9G5BV | IACT |
Source Document#
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| fde4aab7-7b37-4a22-92ec-92bced41e5da | 2f0b7482-4ccd-4375-97d8-56dfe3d8a69b | 2026-05-19 | Warnings | fde4aab7-7b37-4a22-92ec-92bced41e5da 2f0b7482-4ccd-4375-97d8-56dfe3d8a69b |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.