EZ-Quit Control Spray

Manufacturer
Homeocare Laboratories
Effective date
2018-12-31
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:11:02

Label at a glance#

ProductEZ-Quit Control
Active ingredientANTIMONY TRISULFIDE, DIEFFENBACHIA SEGUINE, CADMIUM SULFATE, STRYCHNOS IGNATII SEED, LOBELIA INFLATA, STRYCHNOS NUX-VOMICA SEED, TOBACCO LEAF
Label structure8 sections

Label contents#

Full prescribing information#

Active Ingredients:

OTC - ACTIVE INGREDIENT SECTION

Antimonium crudum 5C, Caladium seg. 5C, Cadmium sulph 5C, Ignatia amara 5C, Lobelia inflata 5C, Nux vomica 5C (Poison nut), Tabacum (Tobacco) 5C-7C-8C.

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Purified water, Ethyl alcohol 20%.

Purpose:

OTC - PURPOSE SECTION

Temporarily relieves cravings for cigarettes & tobacco.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Warnings:

WARNINGS SECTION

If you are pregnant or nursing, or if you have a serious condition, seek the advice of a doctor before using this product. Keep out of the reach of children.

Dosage & Administration:

DOSAGE & ADMINISTRATION SECTION

2 pump-sprays under the tongue, 3 times a day or as needed.

Indications & Usage:

INDICATIONS & USAGE SECTION

2 pump-sprays under the tongue, 3 times a day as needed.

EZ-Quit Control Spray

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

EZ-Quit Control Spray

Homeopathic Medicine

0.5 fl oz. (15 ml)

ez-quit control sprayez-quit control spray

EZ-QUIT-Control-Spray.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
61727-337-15EZ-Quit Control15 mL in 1 BOTTLE, SPRAYSPRAY152

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
61727-337EZ-QUIT CONTROL (ANTIMONY TRISULFIDE, DIEFFENBACHIA SEGUINE, CADMIUM SULFATE, STRYCHNOS IGNATII SEED, LOBELIA INFLATA, STRYCHNOS NUX-VOMICA SEED, TOBACCO LEAF) SPRAY [HOMEOCARE LABORATORIES]2Current NDC, Legacy NDC, 1 package rows20190306_a45f0054-03c6-47e3-abd6-b0a4e37aefbf.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ANTIMONY TRISULFIDEACTIVE INGREDIENTF79059A38U1
CADMIUM SULFATEACTIVE INGREDIENT947UNF3Z6O1
DIEFFENBACHIA SEGUINEACTIVE INGREDIENT01800C6E6B1
LOBELIA INFLATAACTIVE INGREDIENT9PP1T3TC5U1
STRYCHNOS IGNATII SEEDACTIVE INGREDIENT1NM3M2487K1
STRYCHNOS NUX-VOMICA SEEDACTIVE INGREDIENT269XH139191
TOBACCO LEAFACTIVE INGREDIENT6YR2608RSU1
ANTIMONY TRISULFIDEACTIVE MOIETYF79059A38U1
CADMIUM CATIONACTIVE MOIETYT494FZ4G8G1
DIEFFENBACHIA SEGUINEACTIVE MOIETY01800C6E6B1
LOBELIA INFLATAACTIVE MOIETY9PP1T3TC5U1
STRYCHNOS IGNATII SEEDACTIVE MOIETY1NM3M2487K1
STRYCHNOS NUX-VOMICA SEEDACTIVE MOIETY269XH139191
TOBACCO LEAFACTIVE MOIETY6YR2608RSU1
ETHYBENZTROPINEINACTIVE INGREDIENTG1X2X9N95N1
WATERINACTIVE INGREDIENT059QF0KO0R1

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
61727-33761727-337-15

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Source Document#

Source XML · Source PDF

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.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
EZ-Quit ControlANTIMONY TRISULFIDE, DIEFFENBACHIA SEGUINE, CADMIUM SULFATE, STRYCHNOS IGNATII SEED, LOBELIA INFLATA, STRYCHNOS NUX-VOMICA SEED, TOBACCO LEAFHomeocare Laboratoriesa45f0054-03c6-47e3-abd6-b0a4e37aefbf2018-12-31WarningsExact identifier
ndc (package): 61727-337-15
ndc (product): 61727-337
ndc11 (package): 61727033715
spl id: 7e58bc5a-9e32-3e20-e053-2991aa0a4d35
spl set id: a45f0054-03c6-47e3-abd6-b0a4e37aefbf

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.