RUTIN- rutin 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:

Rutin 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C.

HOMEOPATHIC INDICATIONS:

For temporary relief of food and pollen sensitivities including sinusitis, nasal congestion, hay fever, lactose intolerance, and bladder infection.**

**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 physician or Poison Control Center right away.

If pregnant or breast-feeding, ask a health professional before use.

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

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.

INACTIVE INGREDIENTS:

Demineralized Water, 25% Ethanol.

KEEP OUT OF REACH OF CHILDREN:

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

HOMEOPATHIC INDICATIONS:

For temporary relief of food and pollen sensitivities including sinusitis, nasal congestion, hay fever, lactose intolerance, and bladder infection.**

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

QUESTIONS:

Dist. By: Deseret Biologicals, Inc.

469 W. Parkland Drive

Sandy, UT 84070   www.desbio.com

DESBIO

NDC 43742-0211-1

HOMEOPATHIC

RUTIN

1 FL OZ (30 ml)

Rutin

RUTIN 
rutin liquid
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:43742-0211
Route of Administration ORAL
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
RUTIN (UNII: 5G06TVY3R7) (RUTIN - UNII:5G06TVY3R7) RUTIN 6 [hp_X]  in 1 mL
Inactive Ingredients
Ingredient Name Strength
WATER (UNII: 059QF0KO0R)  
ALCOHOL (UNII: 3K9958V90M)  
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:43742-0211-1 30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product 04/26/2017
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved homeopathic 02/27/2012
Labeler - Deseret Biologicals, Inc. (940741853)
Registrant - Apotheca Company (844330915)
Establishment
Name Address ID/FEI Business Operations
Apotheca Company 844330915 manufacture(43742-0211) , api manufacture(43742-0211) , label(43742-0211) , pack(43742-0211)

Revised: 9/2015
Document Id: 6bba7228-e46e-4fa5-b142-70c749f63197
Set id: 4ccdad7d-22ab-426e-b222-0f11a42af56b
Version: 3
Effective Time: 20150917
 
Deseret Biologicals, Inc.