ECHINACEA PURPUREA (N)- echinacea purpurea flowering top tincture

Country: United States

Language: English

Source: NLM (National Library of Medicine)

Active ingredient:

ECHINACEA PURPUREA FLOWERING TOP (UNII: 2EMS3QFX65) (ECHINACEA PURPUREA FLOWERING TOP - UNII:2EMS3QFX65)

Available from:

Phytodyne Inc.

Administration route:

ORAL

Prescription type:

OTC DRUG

Therapeutic indications:

For cold and flu infection and symptoms

Authorization status:

unapproved homeopathic

Summary of Product characteristics

ECHINACEA PURPUREA (N)- ECHINACEA PURPUREA FLOWERING TOP TINCTURE
PHYTODYNE INC.
_Disclaimer: This homeopathic product has not been evaluated by the
Food and Drug_
_Administration for safety or efficacy. FDA is not aware of scientific
evidence to support_
_homeopathy as effective._
----------
ECHINACEA PURPUREA Ø (N)
USE
For cold and flu infection and symptoms
DIRECTIONS
Adults and children above 12 years: 2-5 drops 1-3 times daily in pure
water before
meals. Consult a physician for use in children under 12 years of age.
INGREDIENTS
Echinacea purpurea Ø (N)
ALCOHOL: 65
TAMPER-EVIDENT
Do not use if tamper evident strip is broken from base of cap.
WARNING
Ask a doctor if you are pregnant or nursing.
Keep away from children. In case of overdose, call a medical
professional.
PRINCIPAL DISPLAY PANEL - 20 ML BOTTLE LABEL
CERES
Homeopathic Medicine
Echinacea purpurea Ø (N)
Use: For cold and flu infection and symptoms
Directions : Adults and children above 12 years: 2-5
drops 1-3 times daily in pure water before meals. Consult
a physician for use in children under 12 years of age.
0.67 fl.oz. (20ml)
Lot#:1234567A
®
EXP: 99.9999
ECHINACEA PURPUREA (N)
echinacea purpurea flowering top tincture
PRODUCT INFORMATION
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:13838-1436
ROUTE OF ADMINISTRATION
ORAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRENGTH
ECHINACEA PURPUREA FLOWERING TOP (UNII: 2EMS3QFX65) (ECHINACEA
PURPUREA FLOWERING TOP - UNII:2EMS3QFX65)
ECHINACEA PURPUREA
FLOWERING TOP
1 [hp_X]
in 1 mL
INACTIVE INGREDIENTS
INGREDIENT NAME
STRENGTH
ALCOHOL (UNII: 3K9958V90M)
PACKAGING
# ITEM CODE
PACKAGE DESCRIPTION
MARKETING START
DATE
MARKETING END
DATE
1
NDC:13838-
1436-1
20 mL in 1 BOTTLE, GLASS; Type 0: Not a
Combination Product
10/01/2005
Phytodyne Inc.
MARKETING INFORMATION
MARKETING
CATEGORY
APPLICATION NUMBER OR MONOGRAPH
CITATION
MARKETING START
DATE
MARKETING END
DATE
Unapproved
homeopathic
10/01/2005
LABELER -
Phytodyne Inc. (164980927)
Revised: 12/2021