STO NOSODE 4008- sto nosode 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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N8

ACTIVE INGREDIENTS

all the following at 30X, 60X, 100X:
Chlamydia
Gardnerella
Lymphogranuloma
Medorrhinum
Proteus vulgaris
Pseudomonas
Syphilinum
Trichomonas vaginalis

QUESTIONS

Professional Formulas

PO Box 2034 Lake Oswego, OR 97035

INDICATIONS

For the temporary relief of mild skin rash, itchy skin, changes in urination, chills, joint pain or body aches, nausea, or fatigue.*

*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 sores, blood in urine, or painful urination, 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

20% ethanol, purified water.

LABEL

Est 1985

Professional Formulas

Complementary Health

STO Nosode

Homeopathic Remedy

2 FL. OZ. (59 mL)

Label image

STO NOSODE  4008
sto nosode liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63083-4008
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CHLAMYDIA TRACHOMATIS (UNII: T6NI39QU44) (CHLAMYDIA TRACHOMATIS - UNII:T6NI39QU44) CHLAMYDIA TRACHOMATIS30 [hp_X]  in 59 mL
GARDNERELLA VAGINALIS (UNII: 238RQ26259) (GARDNERELLA VAGINALIS - UNII:238RQ26259) GARDNERELLA VAGINALIS30 [hp_X]  in 59 mL
GONORRHEAL URETHRAL SECRETION HUMAN (UNII: 9BZG9E3I8F) (GONORRHEAL URETHRAL SECRETION HUMAN - UNII:9BZG9E3I8F) GONORRHEAL URETHRAL SECRETION HUMAN30 [hp_X]  in 59 mL
PROTEUS VULGARIS (UNII: 11T9HCO30O) (PROTEUS VULGARIS - UNII:11T9HCO30O) PROTEUS VULGARIS30 [hp_X]  in 59 mL
PSEUDOMONAS AERUGINOSA (UNII: Y793W5V55N) (PSEUDOMONAS AERUGINOSA - UNII:Y793W5V55N) PSEUDOMONAS AERUGINOSA30 [hp_X]  in 59 mL
TREPONEMIC SKIN CANKER HUMAN (UNII: 4ZWP7FWI8W) (TREPONEMIC SKIN CANKER HUMAN - UNII:4ZWP7FWI8W) TREPONEMIC SKIN CANKER HUMAN30 [hp_X]  in 59 mL
TRICHOMONAS VAGINALIS (UNII: Q25X3G314L) (TRICHOMONAS VAGINALIS - UNII:Q25X3G314L) TRICHOMONAS VAGINALIS30 [hp_X]  in 59 mL
Inactive Ingredients
Ingredient NameStrength
ALCOHOL (UNII: 3K9958V90M)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63083-4008-259 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(63083-4008)

Revised: 8/2019
Document Id: ca5c7f29-c165-427b-b76d-73c7a17c2c69
Set id: bf227f2d-62e9-40fa-bbfd-02ee56795953
Version: 1
Effective Time: 20190815
 
Professional Complementary Health Formulas