PREQUIMM (argentum nitricum, colchicum autumnale, conium maculatum, ipecacuanha, nux vomica, pulsatilla- pratensis, veratrum album tablet

Prequimm by

Drug Labeling and Warnings

Prequimm by is a Homeopathic medication manufactured, distributed, or labeled by ZRG Detox, Inc., Apotheca Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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:

Distributed by.

ZRG Detox, Inc.

Calexico, CA 92231

www.zrgdetox.com

1 (877)737-2583

PACKAGE LABEL DISPLAY:

NDC: 62630-002-17

PREQUIMM

TEMPORARILY RELIEVES NAUSEA

AND VOMITING OCCURRING WITH

CHEMOTHERAPY TREATMENTS

HOMEOPATHIC MEDICINE

100TABLETS

INGREDIENTS AND APPEARANCE

PREQUIMM 
argentum nitricum, colchicum autumnale, conium maculatum, ipecacuanha, nux vomica, pulsatilla (pratensis), veratrum album tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62630-002
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SILVER NITRATE (UNII: 95IT3W8JZE) (SILVER CATION - UNII:57N7B0K90A)	SILVER NITRATE	6 [hp_X]
COLCHICUM AUTUMNALE BULB (UNII: 993QHL78E6) (COLCHICUM AUTUMNALE BULB - UNII:993QHL78E6)	COLCHICUM AUTUMNALE BULB	4 [hp_X]
CONIUM MACULATUM FLOWERING TOP (UNII: Q28R5GF371) (CONIUM MACULATUM FLOWERING TOP - UNII:Q28R5GF371)	CONIUM MACULATUM FLOWERING TOP	4 [hp_X]
IPECAC (UNII: 62I3C8233L) (IPECAC - UNII:62I3C8233L)	IPECAC	4 [hp_X]
STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (STRYCHNOS NUX-VOMICA SEED - UNII:269XH13919)	STRYCHNOS NUX-VOMICA SEED	5 [hp_X]
PULSATILLA PRATENSIS WHOLE (UNII: 8E272251DI) (PULSATILLA PRATENSIS WHOLE - UNII:8E272251DI)	PULSATILLA PRATENSIS WHOLE	6 [hp_X]
VERATRUM ALBUM ROOT (UNII: QNS6W5US1Z) (VERATRUM ALBUM ROOT - UNII:QNS6W5US1Z)	VERATRUM ALBUM ROOT	8 [hp_X]

Inactive Ingredients
Ingredient Name	Strength
LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
MAGNESIUM PALMITOSTEARATE (UNII: R4OXA9G5BV)

Product Characteristics
Color	white	Score	no score
Shape	ROUND	Size	10mm
Flavor		Imprint Code	H
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62630-002-17	100 in 1 BOTTLE; Type 0: Not a Combination Product	08/24/2021	08/26/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		08/24/2021	08/26/2026

Labeler - ZRG Detox, Inc. (079301265)

Registrant - Apotheca Company (844330915)

Establishment
Name	Address	ID/FEI	Business Operations
Apotheca Company		844330915	manufacture(62630-002) , api manufacture(62630-002) , label(62630-002) , pack(62630-002)