Cedar Fever
FDA Label NDC 69406-002

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by People's Pharmacy, Inc for the product Cedar Fever (NDC 69406-002). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding active ingredients, uses, keep out of reach of children, indications, warnings, directions, inactive ingredients, principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Active Ingredients

JUNIPERUS VIRGINIANA 6X

ALLIUM CEPA 6X

THUJA LOBBI 6X

GALPHIMIA GLAUCA 6X

FRAX AMER 6X

QUERCUS ROBUR 6X

ULMUS FULVA 6X

Uses

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

Keep Out Of Reach Of Children

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

Indications

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

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

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

20% USP alcohol

Principal Display Panel

Image Description (Cedarfeverdrops)

Image Description (Cedarfeverdrops)

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