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

INDICATIONS

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

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.

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

In case of overdose, contact physician or Poison Control Center right away.

INDICATIONS AND USAGE

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

QUESTIONS

Dist. By: Deseret Biologicals, Inc.

469 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 DEA Schedule     
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
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)

Revised: 2/2013
Document Id: 7ae5e0a1-ee4e-4135-ad1a-c94c0fb80c22
Set id: 4ccdad7d-22ab-426e-b222-0f11a42af56b
Version: 1
Effective Time: 20130227
 
Deseret Biologicals, Inc.