CHENOPODIUM

DRUG FACTS: ACTIVE INGREDIENTS: CHENOPODIUM

CONTENT: Approx. 100 Pellets

USE: To be used according to standard homeopathic indications.

WARNINGS: Keep out of reach of children. If pregnant or breast-feeding, ask a health care professional before use. Stop use and ask a health care professional if symptoms persist for more than 3 days or worsen.

Keep out of reach of children.

DIRECTIONS: Dissolve 3-5 pellets under the tongue 3 times a day or as directed by a professional.

OTHER INFORMATION: Store at room temperature. Do not use if pellet dispenser seal is broken.

INACTIVE INGREDIENTS: Organic sucrose, lactose free.

Manufactured according to the Homeopathic Pharmacopoeia of the United States (HPUS). PRODUCT OF USA.

Mfg. By: OHM PHARMA, INC. Mineral Wells, TX 76067

www.ohmpharma.com FDA Est # 3003231743

CHENOPODIUM

The OTC Potency range from Chenopodium 6X-30X, 3C-30C, 200C, 1M.

Standard bottle sizes for dilution-form can range from 30mL to 60mL.

MD Label

To be used according to standard homeopathic indications.

CHENOPODIUM
chenopodium pellet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:66096-816
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
CHENOPODIUM AMBROSIOIDES (UNII: 4H5RSU087I) (CHENOPODIUM AMBROSIOIDES - UNII:4H5RSU087I)	CHENOPODIUM AMBROSIOIDES	6 [hp_C] in 6 [hp_C]

Ingredient Name	Strength
Inactive Ingredients
SUCROSE (UNII: C151H8M554)

Product Characteristics
Color	white	Score
Shape	ROUND	Size	4mm
Flavor		Imprint Code
Contains

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:66096-816-01	6 [hp_C] in 1 PACKAGE; Type 0: Not a Combination Product	11/01/2019

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved homeopathic		11/01/2019

Labeler - OHM PHARMA INC. (030572478)