Cedar Fever

Manufacturer: People's Pharmacy, Inc | Washington Homeopathic Products
Effective date: 2016-01-27
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: full-release
Hydrated at: 2026-06-01 02:07:30

Label at a glance#

ProductCedar Fever

Active ingredientONION, FRAXINUS AMERICANA BARK, GALPHIMIA GLAUCA FLOWERING TOP, JUNIPERUS VIRGINIANA TWIG, QUERCUS ROBUR TWIG BARK, THUJA PLICATA LEAF, ULMUS RUBRA BARK

Label structure8 sections

Indications and uses

To relieve the symptoms of cedar allergies including sneezing, runny nose, itching eyes and more.

Dosage and administration

Adults (13+) take 30 drops 3 times a day. Repeat as needed or as instructed by a licensed practitioner. Consult a physician for use in children under 12 years of age.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

JUNIPERUS VIRGINIANA 6X

ALLIUM CEPA 6X

THUJA LOBBI 6X

GALPHIMIA GLAUCA 6X

FRAX AMER 6X

QUERCUS ROBUR 6X

ULMUS FULVA 6X

USES

OTC - PURPOSE SECTION

To relieve the symptoms of cedar allergies including sneezing, runny nose, itching eyes and more.

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If you are pregnant or nursing, ask a doctor before use.

INDICATIONS

INDICATIONS & USAGE SECTION

Indications:

JUNIPERUS VIRGINIANA Allergies

ALLIUM CEPA Head cold

THUJA LOBBI Dry, hacking cough

GALPHIMIA GLAUCA Sneezing

FRAX AMER Fever sores on lips

QUERCUS ROBUR Diarrhea

ULMUS FULVA Constipation

WARNINGS

WARNINGS SECTION

Do not use if tamper-resistant seal is missing or broken. Stop use and ask a doctor in cases of high fever or if symptoms persist.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

Adults (13+) take 30 drops 3 times a day. Repeat as needed or as instructed by a licensed practitioner. Consult a physician for use in children under 12 years of age.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

20% USP alcohol

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image description

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
69406-002-11	2020-01-31	C162847	48780-1	9d75b9d0-d837-f424-e053-dadaa90a57ce	DRUG FACTS

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
69406-002-11	Cedar Fever	30 mL in 1 BOTTLE, GLASS	LIQUID	30		3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
69406-002	CEDAR FEVER (ONION - FRAXINUS AMERICANA BARK - GALPHIMIA GLAUCA FLOWERING TOP - JUNIPERUS VIRGINIANA TWIG - QUERCUS ROBUR TWIG BARK - THUJA PLICATA LEAF - ULMUS RUBRA BARK) LIQUID [PEOPLE'S PHARMACY, INC]	3	Legacy NDC, 1 package rows	20160128_e87426fa-0437-49c6-90ab-5e048de9f8c2.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

Cedar Fever
ONION - FRAXINUS AMERICANA BARK - GALPHIMIA GLAUCA FLOWERING TOP - JUNIPERUS VIRGINIANA TWIG - QUERCUS ROBUR TWIG BARK - THUJA PLICATA LEAF - ULMUS RUBRA BARK
ONION
FRAXINUS AMERICANA BARK
GALPHIMIA GLAUCA FLOWERING TOP
JUNIPERUS VIRGINIANA TWIG
QUERCUS ROBUR TWIG BARK
THUJA PLICATA LEAF
ULMUS RUBRA BARK
ALCOHOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
69406-002	69406-002-11

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ONION	492225Q21H	ACTIB
FRAXINUS AMERICANA BARK	0B24UR1O1S	ACTIB
GALPHIMIA GLAUCA FLOWERING TOP	93PH5Q8M7E	ACTIB
JUNIPERUS VIRGINIANA TWIG	532BCG080L	ACTIB
QUERCUS ROBUR TWIG BARK	2JFK226947	ACTIB
THUJA PLICATA LEAF	R9I752FESH	ACTIB
ULMUS RUBRA BARK	91QY4PXU8Q	ACTIB
ALCOHOL	3K9958V90M	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
f0456008-339e-4c07-8e46-6e047d9fcebd			e87426fa-0437-49c6-90ab-5e048de9f8c2	2016-01-27	Warnings	Exact identifier spl id: f0456008-339e-4c07-8e46-6e047d9fcebd spl set id: e87426fa-0437-49c6-90ab-5e048de9f8c2

Reported adverse events (FAERS/openFDA)#

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