SANGUINARIA CAN- sanguinaria canadensis root tablet
Standard Homeopathic Company

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.

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Sanguinaria Can. 30X

Made according to the

Homeopathic Pharmacopoeia

of the United States since 1903.

Warnings

Do not use if cap band is missing or broken.

If you are pregnant or nursing,

consult a licensed beforeusing this product.

If symptoms persist for 7 days or worsen,

contact a licensed practitioner.

Keep this and all medicines out of the reach of children.

To be used according to label

indications and/or standard

homeopathic indications.

Standard Homeopathic Company

Los Angeles, CA 90061

Questions?

800-624-9659

Active Ingredients

SANGUINARIA CAN.

30X

HEADACHE, COLD OR FLU*

Directions

Adults: Disolve 4 tablets under tongue 4 times a day.

Children: Consult a healthcare professional.

In a base of Acacia Gum and Lactose N.F.

Principal Display Panel - 250 Tablet Bottle Label

STANDARD

HOMEOPATHIC

MADE IN THE USA SINCE 1903

NDC # 0360-0396-01

Homeopathic Medicine

SANGUINARIA CAN.

30X

HEADACHE, COLD OR FLU*

*Claims based on traditional homeopathic

practice, not accepted medical evidence.

Not FDA evaluated.

250 TABLETS

label

SANGUINARIA CAN
sanguinaria canadensis root tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:0360-0396
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
SANGUINARIA CANADENSIS ROOT (UNII: N9288CD508) (SANGUINARIA CANADENSIS ROOT - UNII:N9288CD508)	SANGUINARIA CANADENSIS ROOT	30 [hp_X]

Ingredient Name	Strength
Inactive Ingredients
ACACIA (UNII: 5C5403N26O)
LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)

Product Characteristics
Color	white	Score	no score
Shape	ROUND	Size	5mm
Flavor		Imprint Code
Contains

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:0360-0396-01	250 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	02/17/1997

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved homeopathic		02/17/1997	06/29/2023

Labeler - Standard Homeopathic Company (008316655)

Name	Address	ID/FEI	Business Operations
Establishment
Standard Homeopathic Company		008316655	manufacture(0360-0396) , pack(0360-0396) , label(0360-0396)

Revised: 6/2023

Document Id: ff4b5190-6b51-4f95-e053-6294a90ab72e

Set id: 758abf53-ad86-62ac-e053-2991aa0a8f0c

Version: 2

Effective Time: 20230629

Standard Homeopathic Company