RHEUMATISM- benzoicum acidum, pulsatilla, rhododendron chrysanthum, spiraea ulmaria, aconitum napellus, dulcamara, euphorbium officinarum, ledum palustre, asclepias tuberosa, lithium benzoicum, 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.

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DRUG FACTS:

ACTIVE INGREDIENTS:

Benzoicum Acidum 3X, Pulsatilla (Vulgaris) 3X, Rhododendron Chrysanthum 3X, Spiraea Ulmaria 3X, Aconitum Napellus 4X, Dulcamara 4X, Euphorbium Officinarum 4X, Ledum Palustre 4X, Asclepias Tuberosa 6X, Lithium Benzoicum 8X

INDICATIONS:

For temporary relief of symptoms related to rheumatism including joint pain, fever, inflammation and pain of leg(s), gout and numbness in extremities.

WARNINGS:

Keep out of reach of children. In case of overdose, contact 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 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.

INDICATIONS:

For temporary relief of symptoms related to rheumatism including joint pain, fever, inflammation and pain of leg(s), gout and numbness in extremities.

INACTIVE INGREDIENTS:

Demineralized Water, 25% Ethanol.

QUESTIONS:

Dist. By:

Deseret Biologicals, Inc.

469 W. Parkland Drive

Sandy, UT

www.desbio.com

PACKAGE LABEL DISPLAY:

DESBIO

NDC 43742-0001-1

HOMEOPATHIC

RHEUMATISM

1 FL OZ (30 ml)

Rheumatism

RHEUMATISM
benzoicum acidum, pulsatilla, rhododendron chrysanthum, spiraea ulmaria, aconitum napellus, dulcamara, euphorbium officinarum, ledum palustre, asclepias tuberosa, lithium benzoicum, liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:43742-0001
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
BENZOIC ACID (UNII: 8SKN0B0MIM) (BENZOIC ACID - UNII:8SKN0B0MIM)	BENZOIC ACID	3 [hp_X] in 1 mL
PULSATILLA VULGARIS (UNII: I76KB35JEV) (PULSATILLA VULGARIS - UNII:I76KB35JEV)	PULSATILLA VULGARIS	3 [hp_X] in 1 mL
RHODODENDRON AUREUM LEAF (UNII: IV92NQJ73U) (RHODODENDRON AUREUM LEAF - UNII:IV92NQJ73U)	RHODODENDRON AUREUM LEAF	3 [hp_X] in 1 mL
FILIPENDULA ULMARIA ROOT (UNII: 997724QNDS) (FILIPENDULA ULMARIA ROOT - UNII:997724QNDS)	FILIPENDULA ULMARIA ROOT	3 [hp_X] in 1 mL
ACONITUM NAPELLUS (UNII: U0NQ8555JD) (ACONITUM NAPELLUS - UNII:U0NQ8555JD)	ACONITUM NAPELLUS	4 [hp_X] in 1 mL
SOLANUM DULCAMARA FLOWER (UNII: W6J1279A6K) (SOLANUM DULCAMARA FLOWER - UNII:W6J1279A6K)	SOLANUM DULCAMARA FLOWER	4 [hp_X] in 1 mL
EUPHORBIA RESINIFERA RESIN (UNII: 1TI1O9028K) (EUPHORBIA RESINIFERA RESIN - UNII:1TI1O9028K)	EUPHORBIA RESINIFERA RESIN	4 [hp_X] in 1 mL
LEDUM PALUSTRE TWIG (UNII: 877L01IZ0P) (LEDUM PALUSTRE TWIG - UNII:877L01IZ0P)	LEDUM PALUSTRE TWIG	4 [hp_X] in 1 mL
ASCLEPIAS TUBEROSA ROOT (UNII: 1ZL82U5D18) (ASCLEPIAS TUBEROSA ROOT - UNII:1ZL82U5D18)	ASCLEPIAS TUBEROSA ROOT	6 [hp_X] in 1 mL
LITHIUM BENZOATE (UNII: R9Z042Z19E) (LITHIUM CATION - UNII:8H8Z5UER66)	LITHIUM BENZOATE	8 [hp_X] in 1 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:43742-0001-1	30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product	04/05/2012

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved homeopathic		04/05/2012	09/25/2020

Labeler - Deseret Biologicals, Inc. (940741853)

Registrant - Apotheca Company (844330915)

Name	Address	ID/FEI	Business Operations
Establishment
Apotheca Company		844330915	manufacture(43742-0001) , api manufacture(43742-0001) , label(43742-0001) , pack(43742-0001)

Revised: 5/2016

Document Id: 39c22b27-2f78-4d0e-9394-36543c6c4a31

Set id: 0736b300-6357-410c-a860-c0e289c3f8b8

Version: 4

Effective Time: 20160517

Deseret Biologicals, Inc.