STAPH/STREP/RESPIRATORY NOSODE COMBINATION 9418- staph/strep/respiratory nosode combination liquid 
Professional Complementary Health Formulas

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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R418

ACTIVE INGREDIENTS

Aconitum napellus 4X
Bryonia 4X
Phosphorus 5X
Kreosotum 6X
Listeriosis 12X
Staphylococcus aureus 12X
Streptococcus hemolyticus 12X
Streptococcus viridans 12X

QUESTIONS

Professional Formulas

PO Box 2034 Lake Oswego, OR 97035

INDICATIONS

For the temporary relief of runny nose, nasal congestion, sneezing, sore or scratchy throat, or coughing.*

*Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

WARNINGS

Persistent symptoms may be a sign of a serious condition. If symptoms persist or are accompanied by a fever, rash, or persistent headache, consult a doctor. Keep out of the reach of children. In case of overdose, get medical help or contact a poison control center right away. If pregnant or breastfeeding, ask a healthcare professional before use.

Keep out of the reach of children.

If pregnant or breastfeeding, ask a healthcare professional before use.

DIRECTIONS

Place drops under tongue 30 minutes before/after meals. Adults and children 12 years and over: Take 10 to 15 drops once weekly or monthly. If mild symptoms are present, take 10 drops up to 3 times per day. Consult a physician for use in children under 12 years of age.

OTHER INFORMATION

Tamper resistant. If seal is broken, do not use. After opening, close container tightly and store at room temperature away from heat.

INACTIVE INGREDIENTS

40% ethanol, purified water.

LABEL

Est 1985

Professional Formulas

Complementary Health

Staph/Strep/Respiratory Nosode Combination

Homeopathic Remedy

1 FL. OZ. (29.5 mL)

Label image

STAPH/STREP/RESPIRATORY NOSODE COMBINATION  9418
staph/strep/respiratory nosode combination liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63083-9418
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ACONITUM NAPELLUS WHOLE (UNII: U0NQ8555JD) (ACONITUM NAPELLUS WHOLE - UNII:U0NQ8555JD) ACONITUM NAPELLUS WHOLE4 [hp_X]  in 29.5 mL
BRYONIA ALBA ROOT (UNII: T7J046YI2B) (BRYONIA ALBA ROOT - UNII:T7J046YI2B) BRYONIA ALBA ROOT4 [hp_X]  in 29.5 mL
PHOSPHORUS (UNII: 27YLU75U4W) (PHOSPHORUS - UNII:27YLU75U4W) PHOSPHORUS5 [hp_X]  in 29.5 mL
WOOD CREOSOTE (UNII: 3JYG22FD73) (WOOD CREOSOTE - UNII:3JYG22FD73) WOOD CREOSOTE6 [hp_X]  in 29.5 mL
LISTERIA MONOCYTOGENES (UNII: 3O44K14A86) (LISTERIA MONOCYTOGENES - UNII:3O44K14A86) LISTERIA MONOCYTOGENES12 [hp_X]  in 29.5 mL
STAPHYLOCOCCUS AUREUS (UNII: O478WX4004) (STAPHYLOCOCCUS AUREUS - UNII:O478WX4004) STAPHYLOCOCCUS AUREUS12 [hp_X]  in 29.5 mL
STREPTOCOCCUS PYOGENES (UNII: LJ2LP0YL98) (STREPTOCOCCUS PYOGENES - UNII:LJ2LP0YL98) STREPTOCOCCUS PYOGENES12 [hp_X]  in 29.5 mL
Inactive Ingredients
Ingredient NameStrength
ALCOHOL (UNII: 3K9958V90M)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63083-9418-129.5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product08/15/1985
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic08/15/1984
Labeler - Professional Complementary Health Formulas (167339027)
Registrant - Natural Pharmaceutical Manufacturing LLC (015624923)
Establishment
NameAddressID/FEIBusiness Operations
Natural Pharmaceutical Manufacturing LLC015624923manufacture(63083-9418)

Revised: 8/2019
Document Id: b8658595-0464-406e-a01f-526455aa9f7f
Set id: 9981ec07-9bda-4789-9061-9e89de9ee8ed
Version: 1
Effective Time: 20190815
 
Professional Complementary Health Formulas