Label: VERTIGO SYNCOPE DROPS 2115- vertigo syncope drops liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 63083-2115-2 - Packager: Professional Complementary Health Formulas
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved homeopathic
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.
Drug Label Information
Updated August 15, 2019
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- ACTIVE INGREDIENTS
- QUESTIONS
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WARNINGS
Persistent symptoms may be a sign of a serious condition. If symptoms persist or are accompanied by a fever, persistent headache, stiff neck, or changes in vision or hearing, 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.
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DIRECTIONS
Place drops under tongue 30 minutes before/after meals. Adults and children 12 years and over: Take 10 drops up to 3 times per day for up to 6 weeks. For immediate onset of symptoms, take 10 to 15 drops every 15 minutes up to 3 hours. For less severe symptoms, take 10-15 drops hourly up to 8 hours. Consult a physician for use in children under 12 years of age.
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INGREDIENTS AND APPEARANCE
VERTIGO SYNCOPE DROPS 2115
vertigo syncope drops liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63083-2115 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ARNICA MONTANA WHOLE (UNII: O80TY208ZW) (ARNICA MONTANA WHOLE - UNII:O80TY208ZW) ARNICA MONTANA WHOLE 3 [hp_X] in 59 mL CENTELLA ASIATICA LEAF (UNII: 6810070TYD) (CENTELLA ASIATICA LEAF - UNII:6810070TYD) CENTELLA ASIATICA LEAF 3 [hp_X] in 59 mL PHOSPHORIC ACID (UNII: E4GA8884NN) (PHOSPHORIC ACID - UNII:E4GA8884NN) PHOSPHORIC ACID 6 [hp_X] in 59 mL AMBERGRIS (UNII: XTC0D02P6C) (AMBERGRIS - UNII:XTC0D02P6C) AMBERGRIS 12 [hp_X] in 59 mL SILVER NITRATE (UNII: 95IT3W8JZE) (SILVER CATION - UNII:57N7B0K90A) SILVER NITRATE 12 [hp_X] in 59 mL ANAMIRTA COCCULUS FRUIT (UNII: 3E8XBL6YYK) (ANAMIRTA COCCULUS FRUIT - UNII:3E8XBL6YYK) ANAMIRTA COCCULUS FRUIT 12 [hp_X] in 59 mL CONIUM MACULATUM FLOWERING TOP (UNII: Q28R5GF371) (CONIUM MACULATUM FLOWERING TOP - UNII:Q28R5GF371) CONIUM MACULATUM FLOWERING TOP 12 [hp_X] in 59 mL CANIS LUPUS FAMILIARIS MILK (UNII: G39P120JQT) (CANIS LUPUS FAMILIARIS MILK - UNII:G39P120JQT) CANIS LUPUS FAMILIARIS MILK 12 [hp_X] in 59 mL THERIDION CURASSAVICUM (UNII: 9Z8D3HEM8L) (THERIDION CURASSAVICUM - UNII:9Z8D3HEM8L) THERIDION CURASSAVICUM 12 [hp_X] in 59 mL Inactive Ingredients Ingredient Name Strength ALCOHOL (UNII: 3K9958V90M) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:63083-2115-2 59 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product 08/15/1985 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 08/15/1984 Labeler - Professional Complementary Health Formulas (167339027) Registrant - Natural Pharmaceutical Manufacturing LLC (015624923) Establishment Name Address ID/FEI Business Operations Natural Pharmaceutical Manufacturing LLC 015624923 manufacture(63083-2115)
