SMOKE-X

Manufacturer: White Manufacturing Inc. DBA Micro-West | King Bio Homeopathic
Effective date: 2012-12-06
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-06-01 02:04:11

Label at a glance#

ProductSMOKE-X

Active ingredientARSENIC TRIOXIDE, DIEFFENBACHIA SEGUINE, PHENOL, DAPHNE ODORA BARK, SYZYGIUM JAMBOS SEED, POTASSIUM PHOSPHATE, DIBASIC, LOBELIA INFLATA, NICOTINE, STRYCHNOS NUX-VOMICA SEED, PLANTAGO MAJOR, SUCROSE, DELPHINIUM STAPHISAGRIA SEED, TOBACCO LEAF, THUJA OCCIDENTALIS LEAF

Label structure9 sections

Dosage and administration

DIRECTIONS : FOR SELF-HEALING CONDITIONS, TAKE 2 PUMP SPRAYS 3 TIMES DAILY. HOLD UNDER TONGUE 30 SECONDS BEFORE SWALLOWING. MORE FREQUENT DOSAGES MAY BE USED ACCORDING TO SYMPTOMATIC NEEDS

Contacts and useful links#

PhoneLabel contact1-307-358-5066

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

EACH MULTIPLE CONCENTRATES OF 10X, 30X, 100X

ARSENICUM ALBUM [HPUS]
CALADIUM SEGUINUM [HPUS)
CARBOLICUM ACIDUM [HPUS]
DAPHNE INDICA [HPUS]
EUGENIA JAMBOSA [HPUS]
KALI PHOSPHORICUM [HPUS]
LOBELIA INFLATIA
NICOTINUM [HPUS]
NUX VOMICA [HPUS]
PLANTAGO MAJOR [HPUS]
SACCHARUM OFFICINALE [HPUS]
STAPHYSAGRIA [HPUS]
TABACUM [HPUS]
THUJA OCCIDENTALIS

OTC - PURPOSE SECTION

RELIEVES CRAVING FOR TOBACCO SMOKE, CHEWING TOBACCO. HELPS WITH NERVOUSNESS, ANXIETY, IRRITABILITY WHEN QUITTING, COUGH, SHORTNESS OF BREATH, DIFFICULT BREATHING

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN

INDICATIONS & USAGE SECTION

INDICATIONS: RELIEVES CRAVING FOR TOBACCO SMOKE, CHEWING TOBACCO. HELPS WITH NERVOUSNESS, ANXIETY, IRRITABILITY WHEN QUITTING, COUGH, SHORTNESS OF BREATH, DIFFICULT BREATHING

WARNINGS SECTION

WARNING: IF SYMPTOMS PERSIST OR WORSEN, SEEK A PHYSICIANS ADVICE. IF PREGNANT OR NURSING, TAKE ONLY ON ADVICE OF PHYSICIAN. USE ONLY IF TAMPER RESISTANT SEAL IS IN TACT

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

DIRECTIONS: FOR SELF-HEALING CONDITIONS, TAKE 2 PUMP SPRAYS 3 TIMES DAILY. HOLD UNDER TONGUE 30 SECONDS BEFORE SWALLOWING. MORE FREQUENT DOSAGES MAY BE USED ACCORDING TO SYMPTOMATIC NEEDS

INACTIVE INGREDIENT SECTION

POTASSIUM SORBATE AS STABILIZER

MANUFACTURE

SPL UNCLASSIFIED SECTION

MANUFACTURED FOR MICRO-WEST

DOUGLAS, WY 82633

1-307-358-5066

LABEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

IMAGE OF BOTTLE LABEL

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
efd58dcf-540a-4531-8766-e713129ca6f2	Product name	1	20250307
4b7700e3-6e0e-45e5-9d22-6f754d61386e	Product name	2	20250304
726062af-1135-4707-a1d7-57256991bbf9	Product name	2	20250226
63f39a63-5cd1-4016-bd86-2bbb0f6c3139	Product name	3	20240506
e5a77e9c-c528-733a-173d-914a234c024b	Product name	5	20240506
7cda52fc-125f-421c-8fea-bc1974370c49	Product name	2	20180703
0ca1d589-929b-4b33-bc5b-1d84abdafa6a	Product name	1	20150324
fc363c46-397b-4476-ac0f-70e43e8e4592	Product name	1	20150324
19c71a3d-ed9c-166b-a7e5-38c250c35631	Product name	1	20140508
dbebfdf8-6e0c-cfa8-fdbc-e5d7f1bf1562	Product name	1	20140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
61657-0915-1	2020-01-31	C162847	48780-1	9d75b9d1-17af-f424-e053-dadaa90a57ce	DRUG FACTS

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
61657-0915-1	SMOKE-X	30 mL in 1 BOTTLE, PUMP	LIQUID	30		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
61657-0915	SMOKE-X (ARSENICUM ALBUM,PLANTAGO MAJOR,THUJA OCCIDENTALIS,TABACUM,STAPHYSAGRIA,SACCHARUM OFFICINALE,DAPHNE INDICA,NUX VOMICA,NICOTINUM,LOBELIA INFLATA,KALI PHOSPHORICUM,EUGENIA JAMBOSA,CARBOLICUM ACIDUM,CALADIUM SEGUINUM,) LIQUID [WHITE MANUFACTURING INC. DBA MICRO-WEST]	2	Legacy NDC, 1 package rows	20121207_f4fc1591-b501-468f-bc36-254a7a3e0fdd.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
ARSENIC TRIOXIDE	ACTIVE INGREDIENT	S7V92P67HO	2
DAPHNE ODORA BARK	ACTIVE INGREDIENT	JSJ34YQJ5D	2
DELPHINIUM STAPHISAGRIA SEED	ACTIVE INGREDIENT	00543AP1JV	2
DIEFFENBACHIA SEGUINE	ACTIVE INGREDIENT	01800C6E6B	2
LOBELIA INFLATA	ACTIVE INGREDIENT	9PP1T3TC5U	2
NICOTINE	ACTIVE INGREDIENT	6M3C89ZY6R	2
PHENOL	ACTIVE INGREDIENT	339NCG44TV	2
PLANTAGO MAJOR	ACTIVE INGREDIENT	W2469WNO6U	2
POTASSIUM PHOSPHATE, DIBASIC	ACTIVE INGREDIENT	CI71S98N1Z	2
STRYCHNOS NUX-VOMICA SEED	ACTIVE INGREDIENT	269XH13919	2
SUCROSE	ACTIVE INGREDIENT	C151H8M554	2
SYZYGIUM JAMBOS SEED	ACTIVE INGREDIENT	97P0H45869	2
THUJA OCCIDENTALIS LEAF	ACTIVE INGREDIENT	0T0DQN8786	2
TOBACCO LEAF	ACTIVE INGREDIENT	6YR2608RSU	2
ARSENIC CATION (3)	ACTIVE MOIETY	C96613F5AV	2
DAPHNE ODORA BARK	ACTIVE MOIETY	JSJ34YQJ5D	2
DELPHINIUM STAPHISAGRIA SEED	ACTIVE MOIETY	00543AP1JV	2
DIEFFENBACHIA SEGUINE	ACTIVE MOIETY	01800C6E6B	2
LOBELIA INFLATA	ACTIVE MOIETY	9PP1T3TC5U	2
NICOTINE	ACTIVE MOIETY	6M3C89ZY6R	2
PHENOL	ACTIVE MOIETY	339NCG44TV	2
PHOSPHATE ION	ACTIVE MOIETY	NK08V8K8HR	2
PLANTAGO MAJOR	ACTIVE MOIETY	W2469WNO6U	2
STRYCHNOS NUX-VOMICA SEED	ACTIVE MOIETY	269XH13919	2
SUCROSE	ACTIVE MOIETY	C151H8M554	2
SYZYGIUM JAMBOS SEED	ACTIVE MOIETY	97P0H45869	2
THUJA OCCIDENTALIS LEAF	ACTIVE MOIETY	0T0DQN8786	2
TOBACCO LEAF	ACTIVE MOIETY	6YR2608RSU	2
POTASSIUM SORBATE	INACTIVE INGREDIENT	1VPU26JZZ4	2

Products#

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

DailyMed product names page 1 of 1 · 19 matching rows.

SMOKE-X
ARSENICUM ALBUM,PLANTAGO MAJOR,THUJA OCCIDENTALIS,TABACUM,STAPHYSAGRIA,SACCHARUM OFFICINALE,DAPHNE INDICA,NUX VOMICA,NICOTINUM,LOBELIA INFLATA,KALI PHOSPHORICUM,EUGENIA JAMBOSA,CARBOLICUM ACIDUM,CALADIUM SEGUINUM,
ARSENIC TRIOXIDE
ARSENIC CATION (3)
DIEFFENBACHIA SEGUINE
PHENOL
DAPHNE ODORA BARK
SYZYGIUM JAMBOS SEED
POTASSIUM PHOSPHATE, DIBASIC
PHOSPHATE ION
LOBELIA INFLATA
NICOTINE
STRYCHNOS NUX-VOMICA SEED
PLANTAGO MAJOR
SUCROSE
DELPHINIUM STAPHISAGRIA SEED
TOBACCO LEAF
THUJA OCCIDENTALIS LEAF
POTASSIUM SORBATE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
61657-0915	61657-0915-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ARSENIC TRIOXIDE	S7V92P67HO	ACTIB
DIEFFENBACHIA SEGUINE	01800C6E6B	ACTIB
PHENOL	339NCG44TV	ACTIB
DAPHNE ODORA BARK	JSJ34YQJ5D	ACTIB
SYZYGIUM JAMBOS SEED	97P0H45869	ACTIB
POTASSIUM PHOSPHATE, DIBASIC	CI71S98N1Z	ACTIB
LOBELIA INFLATA	9PP1T3TC5U	ACTIB
NICOTINE	6M3C89ZY6R	ACTIB
STRYCHNOS NUX-VOMICA SEED	269XH13919	ACTIB
PLANTAGO MAJOR	W2469WNO6U	ACTIB
SUCROSE	C151H8M554	ACTIB
DELPHINIUM STAPHISAGRIA SEED	00543AP1JV	ACTIB
TOBACCO LEAF	6YR2608RSU	ACTIB
THUJA OCCIDENTALIS LEAF	0T0DQN8786	ACTIB
POTASSIUM SORBATE	1VPU26JZZ4	IACT

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 19 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredient	IID ingredient	UNII	Dosage form / route	Potency	Maximum daily exposure	Match
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	SOLUTION / RECTAL	6.67 %w/v		Exact identifier — unii candidate 19 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	SOLUTION/ DROPS / OPHTHALMIC	0.47 %w/v		Exact identifier — unii candidate 19 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	PASTE / ORAL		48 mg	Exact identifier — unii candidate 19 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	LOTION / TOPICAL	0.2 %w/w		Exact identifier — unii candidate 19 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	TABLET, FILM COATED, EXTENDED RELEASE / ORAL	0.2 mg		Exact identifier — unii candidate 19 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	GRANULE, FOR SUSPENSION / ORAL		80 mg	Exact identifier — unii candidate 19 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	CREAM / TOPICAL	0.25 %w/w		Exact identifier — unii candidate 19 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	CAPSULE / ORAL	NA		Exact identifier — unii candidate 19 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	EMULSION / OPHTHALMIC	0.47 %w/v		Exact identifier — unii candidate 19 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	SYRUP / ORAL	2 mg/1ml		Exact identifier — unii candidate 19 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	SPRAY, METERED / NASAL	0.06 mg		Exact identifier — unii candidate 19 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	CONCENTRATE / ORAL		1 mg	Exact identifier — unii candidate 19 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	TABLET / ORAL		6 mg	Exact identifier — unii candidate 19 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	POWDER, FOR SUSPENSION / ORAL		19 mg	Exact identifier — unii candidate 19 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	TABLET, COATED / ORAL	NA		Exact identifier — unii candidate 19 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	SOLUTION / ORAL	1000 mg/15ml		Exact identifier — unii candidate 19 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	AEROSOL, FOAM / TOPICAL		8 mg	Exact identifier — unii candidate 19 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	SUSPENSION / ORAL		400 mg	Exact identifier — unii candidate 19 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	TABLET, EXTENDED RELEASE / ORAL	0.2 mg		Exact identifier — unii candidate 19 equally ranked IID candidates

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
6a2bb31c-4326-4bbf-85f3-932a0af4dd28			f4fc1591-b501-468f-bc36-254a7a3e0fdd	2012-12-06	Warnings	Exact identifier spl id: 6a2bb31c-4326-4bbf-85f3-932a0af4dd28 spl set id: f4fc1591-b501-468f-bc36-254a7a3e0fdd

Reported adverse events (FAERS/openFDA)#

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