Sulphur Remedy: Homeopathic Product Information

SULPHUR REMEDY- sulfur, asclepias tuberosa root, bryonia alba root and solanum dulcamara stem liquid
Deseret Biologicals, 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.

ACTIVE INGREDIENTS:

Sulphur 4X, 10X, Asclepias Tuberosa 6X, 10X, 30X, Bryonia 10X, 30X, Dulcamara 10X, 30X.

HOMEOPATHIC INDICATIONS:

For temporary relief of symptoms such as headache, fever, muscle aches, skin inflammation.**

**These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

WARNINGS:

Keep out of reach of children. In case of overdose, contact a physician or Poison Control Center right away.

If pregnant or breast-feeding, seek advice of a health professional before use.

Tamper seal: “Sealed for Your Protection.” Do not use if seal is broken or missing.

KEEP OUT OF REACH OF CHILDREN:

Keep out of reach of children. In case of overdose, contact a physician or Poison Control Center right away.

DIRECTIONS:

1-10 drops under the tongue, 3 times a day or as directed by a health professional. Consult a physician for use in children under 12 years of age.

HOMEOPATHIC INDICATIONS:

For temporary relief of symptoms such as headache, fever, muscle aches, skin inflammation.**

**These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

INACTIVE INGREDIENTS:

Demineralized Water, 25% Ethanol.

QUESTIONS:

Dist. By: Deseret Biologicals, Inc.

469 W. Parkland Drive

Sandy, UT 84070 www.desbio.com

PACKAGE LABEL DISPLAY:

DESBIO

NDC 43742-0745-1

HOMEOPATHIC

SULPHUR

REMEDY

1 FL OZ (30 ml)

Sulphur Remedy
(click image for full-size original)
SULPHUR REMEDY
sulphur, asclepias tuberosa, bryonia, dulcamara liquid
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:43742-0745
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
SULFUR (SULFUR) SULFUR 4 [hp_X] in 1 mL
ASCLEPIAS TUBEROSA ROOT (ASCLEPIAS TUBEROSA ROOT) ASCLEPIAS TUBEROSA ROOT 6 [hp_X] in 1 mL
BRYONIA ALBA ROOT (BRYONIA ALBA ROOT) BRYONIA ALBA ROOT 10 [hp_X] in 1 mL
SOLANUM DULCAMARA STEM (SOLANUM DULCAMARA STEM) SOLANUM DULCAMARA STEM 10 [hp_X] in 1 mL
Inactive Ingredients
Ingredient Name Strength
WATER
ALCOHOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:43742-0745-1 30 mL in 1 BOTTLE, DROPPER None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved homeopathic 05/04/2016
Labeler — Deseret Biologicals, Inc. (940741853)
Registrant — Apotheca Company (844330915)
Establishment
Name Address ID/FEI Operations
Apotheca Company 844330915 manufacture (43742-0745), api manufacture (43742-0745), label (43742-0745), pack (43742-0745)

Revised: 05/2017 Deseret Biologicals, Inc.

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