Total FLU-CLD 1

Manufacturer: White Manufacturing Inc. DBA Micro-West | King Bio Inc
Effective date: 2014-08-20
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-06-01 02:05:57

Label at a glance#

ProductTotal FLU-CLD 1

Active ingredientARSENIC TRIOXIDE, BAPTISIA TINCTORIA ROOT, BRYONIA ALBA ROOT, CAUSTICUM, CINCHONA OFFICINALIS BARK, SOLANUM DULCAMARA FLOWER, EUPATORIUM PERFOLIATUM FLOWERING TOP, ECHINACEA PURPUREA, EUCALYPTUS GLOBULUS LEAF, GELSEMIUM SEMPERVIRENS ROOT, LACHESIS MUTA VENOM, PHYTOLACCA AMERICANA ROOT, TOXICODENDRON PUBESCENS LEAF, LACTIC ACID, L-, SULFUR, WYETHIA HELENIOIDES ROOT, INFLUENZA A VIRUS, CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE

Label structure10 sections

Dosage and administration

DIRECTIONS: ONE SPRAY UP EACH NOSTRIL 3 TIMES A DAY. For ages 2 to adult

Contacts and useful links#

PhoneLabel contact1-307-358-5066

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

Contains equal volumes of each ingredient in 10X, 30X, 100X potencies:

Arsenicum alb
Baptisia
Bryonia
Causticum
Cinchona
Dulcamara
Eupatorium perf

Echinacea purp

Eucalyptus

Gelsemium

Influenzinum

Lachesis

Phytolacca

Rhus tox

Sarcolacticum ac

Sulphur

Wyethia

Anas barb in 35C, 50C,100C potencies

PURPOSE

OTC - PURPOSE SECTION

For a broad spectrum of flu-like symptoms including fever, chills, night sweats, nausea, vomiting, headache, runny nose, congestion, sore throat, cough, diarrhea, and tired, achy feeling

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN

INDICATIONS

INDICATIONS & USAGE SECTION

INDICATIONS: For the temporary refief of a broad spectrum of flu-like symptoms including fever, chills, night sweats, nausea, vomiting, headache, runny nose, congestion, sore throat, cough, bronchitis, diarrhea, and tired, achy feeling

WARNINGS SECTION

WARNING: STOP USE AND CALL A DOCTOR if symptoms persist or worsen. CONTAINS ALCOHOL: in case of accidental overdose, consult a poison control center immediately

OTHER INFORMATION: Tamper resistant for your protection. Use only if safety seal is intact.

PREGNANT

OTC - PREGNANCY OR BREAST FEEDING SECTION

IF PREGNANT OR BREAST FEEDING, consult a healthcare professional before use.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

DIRECTIONS: ONE SPRAY UP EACH NOSTRIL 3 TIMES A DAY. For ages 2 to adult

INACTIVE INGREDIENT SECTION

SALINE SOLUTION BASE

MANUFACTURE

SPL UNCLASSIFIED SECTION

MANUFACTURED FOR

MICRO-WEST

P. O. Box 950

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
63f39a63-5cd1-4016-bd86-2bbb0f6c3139	Product name	3	20240506
e5a77e9c-c528-733a-173d-914a234c024b	Product name	5	20240506

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
61657-0968-1	2020-01-31	C162847	48780-1	9d75b9d0-f868-f424-e053-dadaa90a57ce	DRUG FACTS

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
61657-0968-1	Total FLU-CLD 1	30 mL in 1 BOTTLE, WITH APPLICATOR	LIQUID	30		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
61657-0968	TOTAL FLU-CLD 1 (ARSENICUM ALBUM,SULPHUR,ANAS BARBARIAE,WYETHIA HELENIOIDES,SARCOLACTICUM ACIDUM,RHUS TOXICODENDRON,PHYTOLACCA DECANDRA,LACHESIS MUTUS,GELSEMIUM SEMPERVIRENS,EUCALYPTUS GLOBULUS,ECHINACEA PURPUREA,EUPATORIUM PERFOLIATUM,DULCAMARA,,CINCHONA OFFICINALIS,BRYONIA ALBA,CAUSTICUM,BAPTISIA TINCTORIA,) LIQUID [WHITE MANUFACTURING INC. DBA MICRO-WEST]	2	Legacy NDC, 1 package rows	20140828_2cda1532-1007-4afc-b5e1-cfa1f5349190.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
ARSENIC TRIOXIDE	ACTIVE INGREDIENT	S7V92P67HO	2
BAPTISIA TINCTORIA ROOT	ACTIVE INGREDIENT	5EF0HWI5WU	2
BRYONIA ALBA ROOT	ACTIVE INGREDIENT	T7J046YI2B	2
CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE	ACTIVE INGREDIENT	RN2HC612GY	2
CAUSTICUM	ACTIVE INGREDIENT	DD5FO1WKFU	2
CINCHONA OFFICINALIS BARK	ACTIVE INGREDIENT	S003A158SB	2
ECHINACEA PURPUREA	ACTIVE INGREDIENT	QI7G114Y98	2
EUCALYPTUS GLOBULUS LEAF	ACTIVE INGREDIENT	S546YLW6E6	2
EUPATORIUM PERFOLIATUM FLOWERING TOP	ACTIVE INGREDIENT	1W0775VX6E	2
GELSEMIUM SEMPERVIRENS ROOT	ACTIVE INGREDIENT	639KR60Q1Q	2
INFLUENZA A VIRUS	ACTIVE INGREDIENT	R9HH0NDE2E	2
LACHESIS MUTA VENOM	ACTIVE INGREDIENT	VSW71SS07I	2
LACTIC ACID, L-	ACTIVE INGREDIENT	F9S9FFU82N	2
PHYTOLACCA AMERICANA ROOT	ACTIVE INGREDIENT	11E6VI8VEG	2
SOLANUM DULCAMARA FLOWER	ACTIVE INGREDIENT	W6J1279A6K	2
SULFUR	ACTIVE INGREDIENT	70FD1KFU70	2
TOXICODENDRON PUBESCENS LEAF	ACTIVE INGREDIENT	6IO182RP7A	2
WYETHIA HELENIOIDES ROOT	ACTIVE INGREDIENT	J10PD1AQ0N	2
ARSENIC CATION (3+)	ACTIVE MOIETY	C96613F5AV	2
BAPTISIA TINCTORIA ROOT	ACTIVE MOIETY	5EF0HWI5WU	2
BRYONIA ALBA ROOT	ACTIVE MOIETY	T7J046YI2B	2
CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE	ACTIVE MOIETY	RN2HC612GY	2
CAUSTICUM	ACTIVE MOIETY	DD5FO1WKFU	2
CINCHONA OFFICINALIS BARK	ACTIVE MOIETY	S003A158SB	2
ECHINACEA PURPUREA	ACTIVE MOIETY	QI7G114Y98	2
EUCALYPTUS GLOBULUS LEAF	ACTIVE MOIETY	S546YLW6E6	2
EUPATORIUM PERFOLIATUM FLOWERING TOP	ACTIVE MOIETY	1W0775VX6E	2
GELSEMIUM SEMPERVIRENS ROOT	ACTIVE MOIETY	639KR60Q1Q	2
INFLUENZA A VIRUS	ACTIVE MOIETY	R9HH0NDE2E	2
LACHESIS MUTA VENOM	ACTIVE MOIETY	VSW71SS07I	2
LACTIC ACID, L-	ACTIVE MOIETY	F9S9FFU82N	2
PHYTOLACCA AMERICANA ROOT	ACTIVE MOIETY	11E6VI8VEG	2
SOLANUM DULCAMARA FLOWER	ACTIVE MOIETY	W6J1279A6K	2
SULFUR	ACTIVE MOIETY	70FD1KFU70	2
TOXICODENDRON PUBESCENS LEAF	ACTIVE MOIETY	6IO182RP7A	2
WYETHIA HELENIOIDES ROOT	ACTIVE MOIETY	J10PD1AQ0N	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 · 22 matching rows.

Total FLU-CLD 1
ARSENICUM ALBUM,SULPHUR,ANAS BARBARIAE,WYETHIA HELENIOIDES,SARCOLACTICUM ACIDUM,RHUS TOXICODENDRON,PHYTOLACCA DECANDRA,LACHESIS MUTUS,GELSEMIUM SEMPERVIRENS,EUCALYPTUS GLOBULUS,ECHINACEA PURPUREA,EUPATORIUM PERFOLIATUM,DULCAMARA,,CINCHONA OFFICINALIS,BRYONIA ALBA,CAUSTICUM,BAPTISIA TINCTORIA,
ARSENIC TRIOXIDE
ARSENIC CATION (3+)
BAPTISIA TINCTORIA ROOT
BRYONIA ALBA ROOT
CAUSTICUM
CINCHONA OFFICINALIS BARK
SOLANUM DULCAMARA FLOWER
EUPATORIUM PERFOLIATUM FLOWERING TOP
ECHINACEA PURPUREA
EUCALYPTUS GLOBULUS LEAF
GELSEMIUM SEMPERVIRENS ROOT
LACHESIS MUTA VENOM
PHYTOLACCA AMERICANA ROOT
TOXICODENDRON PUBESCENS LEAF
LACTIC ACID, L-
SULFUR
WYETHIA HELENIOIDES ROOT
INFLUENZA A VIRUS
CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE
POTASSIUM SORBATE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
61657-0968	61657-0968-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 19 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ARSENIC TRIOXIDE	S7V92P67HO	ACTIB
BAPTISIA TINCTORIA ROOT	5EF0HWI5WU	ACTIB
BRYONIA ALBA ROOT	T7J046YI2B	ACTIB
CAUSTICUM	DD5FO1WKFU	ACTIB
CINCHONA OFFICINALIS BARK	S003A158SB	ACTIB
SOLANUM DULCAMARA FLOWER	W6J1279A6K	ACTIB
EUPATORIUM PERFOLIATUM FLOWERING TOP	1W0775VX6E	ACTIB
ECHINACEA PURPUREA	QI7G114Y98	ACTIB
EUCALYPTUS GLOBULUS LEAF	S546YLW6E6	ACTIB
GELSEMIUM SEMPERVIRENS ROOT	639KR60Q1Q	ACTIB
LACHESIS MUTA VENOM	VSW71SS07I	ACTIB
PHYTOLACCA AMERICANA ROOT	11E6VI8VEG	ACTIB
TOXICODENDRON PUBESCENS LEAF	6IO182RP7A	ACTIB
LACTIC ACID, L-	F9S9FFU82N	ACTIB
SULFUR	70FD1KFU70	ACTIB
WYETHIA HELENIOIDES ROOT	J10PD1AQ0N	ACTIB
INFLUENZA A VIRUS	R9HH0NDE2E	ACTIB
CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE	RN2HC612GY	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	CONCENTRATE / ORAL		1 mg	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	SOLUTION / RECTAL	6.67 %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	PASTE / ORAL		48 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	LOTION / TOPICAL	0.2 %w/w		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, FILM COATED, EXTENDED RELEASE / ORAL	0.2 mg		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	TABLET, COATED / ORAL	NA		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	CREAM / TOPICAL	0.25 %w/w		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	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	SPRAY, METERED / NASAL	0.06 mg		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	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
ed7f4671-62cf-4f14-891d-71e6bab5eee8			2cda1532-1007-4afc-b5e1-cfa1f5349190	2014-08-20	Warnings	Exact identifier spl id: ed7f4671-62cf-4f14-891d-71e6bab5eee8 spl set id: 2cda1532-1007-4afc-b5e1-cfa1f5349190

Reported adverse events (FAERS/openFDA)#

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