Label: NECTADYN- drosera rotundifolia and ipecac and rumex crispus root and antimony potassium tartrate and cupric sulfate and spongia officinalis skeleton, roasted syrup
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Contains inactivated NDC Code(s)
NDC Code(s): 50114-8510-1 - Packager: Heel Inc
- 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 January 15, 2013
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
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PURPOSE
Drosera rotundifolia 4X.....................Relieves cough
Ipecacuanha 4X................................Relieves chest congestion
Rumex crispus 4X..............................Relieves tickling cough
Antimonium tartaricum 6X..................Relieves chest congestion
Cuprum sulphuricum 6X....................Relieves cough
Spongia tosta 8X..............................Relieves dry cough
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS AND USAGE
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WARNINGS
Stop and ask a doctor if:
If symptoms persist for more than 7 days, comes back, or occurs with fever, rash or headache that lasts. These could be signs of a serious condition. Do not use if known sensitivity to Nectadyn or any of its ingredients exists.
If pregnant or breast-feeding, ask a healthcare provider before use.
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DOSAGE AND ADMINISTRATION
Directions: Adults and children 12 and over
Standard Dosage:1-2 teaspoons every 4 to 6 hours up to 12 teaspoons per day
Directions: Children 4- 11 years
Standard Dosage:1 teaspoon every 2-3 hours up to 6 teaspoons per day
Directions: Children under 4 years
Standard Dosage:Consult a healthcare provider
- ACTIVE INGREDIENTS
- INACTIVE INGREDIENTS
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
NECTADYN
drosera rotundifolia and ipecac and rumex crispus root and antimony potassium tartrate and cupric sulfate and spongia officinalis skeleton, roasted syrupProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:50114-8510 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DROSERA ROTUNDIFOLIA (UNII: QR44N9XPJQ) (DROSERA ROTUNDIFOLIA - UNII:QR44N9XPJQ) DROSERA ROTUNDIFOLIA 4 [hp_X] in 125 mL IPECAC (UNII: 62I3C8233L) (IPECAC - UNII:62I3C8233L) IPECAC 4 [hp_X] in 125 mL RUMEX CRISPUS ROOT (UNII: 9N1RM2S62C) (RUMEX CRISPUS ROOT - UNII:9N1RM2S62C) RUMEX CRISPUS ROOT 4 [hp_X] in 125 mL ANTIMONY POTASSIUM TARTRATE (UNII: DL6OZ476V3) (ANTIMONY CATION (3+) - UNII:069647RPT5) ANTIMONY POTASSIUM TARTRATE 6 [hp_X] in 125 mL CUPRIC SULFATE (UNII: LRX7AJ16DT) (CUPRIC CATION - UNII:8CBV67279L) CUPRIC SULFATE 6 [hp_X] in 125 mL SPONGIA OFFICINALIS SKELETON, ROASTED (UNII: 1PIP394IID) (SPONGIA OFFICINALIS SKELETON, ROASTED - UNII:1PIP394IID) SPONGIA OFFICINALIS SKELETON, ROASTED 8 [hp_X] in 125 mL Inactive Ingredients Ingredient Name Strength HONEY (UNII: Y9H1V576FH) WATER (UNII: 059QF0KO0R) SUCROSE (UNII: C151H8M554) LEMON OIL (UNII: I9GRO824LL) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) METHYLPARABEN (UNII: A2I8C7HI9T) PROPYLPARABEN (UNII: Z8IX2SC1OH) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:50114-8510-1 1 in 1 CARTON 1 125 mL in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 08/31/2007 Labeler - Heel Inc (102783016) Establishment Name Address ID/FEI Business Operations Heel Belgium 282761204 manufacture(50114-8510)
