UPPER RESPIRATORY STAPH STEP COMBINATION- staphylococcus aureus, klebsiella pneumoniae, enterococcus faecalis, pneumococcinum, streptococcus agalactiae, streptococcus mutans, haemophilus influenzae b, streptococcus viridans liquid

Upper Respiratory Staph Step Combination by

Drug Labeling and Warnings

Upper Respiratory Staph Step Combination by is a Homeopathic medication manufactured, distributed, or labeled by Deseret Biologicals, Inc., Apotheca Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENTS:

Staphylococcus Aureus 15X, 30X, 60X, 200X, Klebsiella Pneumoniae 15X, 30X, 200X, 12C, 30C, 60C, 200C, Enterococcus Faecalis 12C, 30C, 60C, 200C, Pneumococcinum 12C, 30C, 60C, 200C, Streptococcus Agalactiae 12C, 30C, 60C, 200C, Streptococcus Mutans 12C, 30C, 60C, 200C, Haemophilus Influenzae B 12C, 60C, 200C,  Streptococcus Viridans 36C, 60C, 200C.

HOMEOPATHIC INDICATIONS:

For temporary relief of symptoms related to upper respiratory infections including fever, irritated throat, swollen glands, inflamed sinus, cough and runny nose.**

**These statements are based upon traditional 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, get medical help or contact a Poison Control Center right away.

INDICATIONS:

For temporary relief of symptoms related to upper respiratory infections including fever, irritated throat, swollen glands, inflamed sinus, cough and runny nose.**

**These statements are based upon traditional 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

PACKAGE LABEL DISPLAY:

DESBIO 

NDC: 43742-0162-1

HOMEOPATHIC

UPPER RESPIRATORY

STAPH STREP

COMBINATION

1 FL OZ (30 ml)

INGREDIENTS AND APPEARANCE

UPPER RESPIRATORY STAPH STEP COMBINATION 
staphylococcus aureus, klebsiella pneumoniae, enterococcus faecalis, pneumococcinum, streptococcus agalactiae, streptococcus mutans, haemophilus influenzae b, streptococcus viridans liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 43742-0162
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
STAPHYLOCOCCUS AUREUS (UNII: O478WX4004) (STAPHYLOCOCCUS AUREUS - UNII:O478WX4004)	STAPHYLOCOCCUS AUREUS	15 [hp_X]  in 1 mL
KLEBSIELLA PNEUMONIAE (UNII: 09PA36CT5R) (KLEBSIELLA PNEUMONIAE - UNII:09PA36CT5R)	KLEBSIELLA PNEUMONIAE	15 [hp_X]  in 1 mL
ENTEROCOCCUS FAECALIS (UNII: 15E04LZ9CT) (ENTEROCOCCUS FAECALIS - UNII:15E04LZ9CT)	ENTEROCOCCUS FAECALIS	12 [hp_C]  in 1 mL
STREPTOCOCCUS PNEUMONIAE (UNII: BT6U234YR2) (STREPTOCOCCUS PNEUMONIAE - UNII:BT6U234YR2)	STREPTOCOCCUS PNEUMONIAE	12 [hp_C]  in 1 mL
STREPTOCOCCUS AGALACTIAE (UNII: 2B3763S671) (STREPTOCOCCUS AGALACTIAE - UNII:2B3763S671)	STREPTOCOCCUS AGALACTIAE	12 [hp_C]  in 1 mL
STREPTOCOCCUS MUTANS (UNII: 5C7J33MJJ1) (STREPTOCOCCUS MUTANS - UNII:5C7J33MJJ1)	STREPTOCOCCUS MUTANS	12 [hp_C]  in 1 mL
HAEMOPHILUS INFLUENZAE TYPE B (UNII: F2TW0N64FI) (HAEMOPHILUS INFLUENZAE TYPE B - UNII:F2TW0N64FI)	HAEMOPHILUS INFLUENZAE TYPE B	12 [hp_C]  in 1 mL
STREPTOCOCCUS VIRIDANS GROUP (UNII: NNV2379HKR) (STREPTOCOCCUS VIRIDANS GROUP - UNII:NNV2379HKR)	STREPTOCOCCUS VIRIDANS GROUP	12 [hp_C]  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: 43742-0162-1	30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product	09/10/2012	06/01/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		09/10/2012	06/01/2021

Labeler - Deseret Biologicals, Inc. (940741853)

Registrant - Apotheca Company (844330915)

Establishment
Name	Address	ID/FEI	Business Operations
Apotheca Company		844330915	manufacture(43742-0162) , api manufacture(43742-0162) , label(43742-0162) , pack(43742-0162)