Label: NYLOXIN STAGE 3 PAIN RELIEF- naja naja venom spray, metered
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Contains inactivated NDC Code(s)
NDC Code(s): 47219-251-10 - Packager: RECEPTOPHARM 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 November 30, 2009
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredients
- Purpose
- INDICATIONS & USAGE
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Warnings:
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- Side effects may include headahce, nausea, sore throat, allergic rhinitis and gastointestinal upset.
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- If symptoms persist or worsen, stop using this product and consult a physician.
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- When Using This Product: avoid contact with the eyes. If product gets into eyes, flush with water. Seek medical attention.
- Directions For Use:
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Other Information:
- Do not use if tamper-proof seal is broken.
- This product is NOT intended to treat disease, it can provide a temporary level of comfort, relief and a feeling of wellness.
- This product has been determined to be safe and effective for moderate to severe (Stage 2) pain.
- Clinical experience suggests Nyloxin may provide relief from other forms of pain.
- SPL UNCLASSIFIED SECTION
- Inactive Ingredients:
- PRINCIPAL DISPLAY PANEL
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
NYLOXIN STAGE 3 PAIN RELIEF
naja naja venom spray, meteredProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:47219-251 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NAJA NAJA VENOM (UNII: ZZ4AG7L7VM) (NAJA NAJA VENOM - UNII:ZZ4AG7L7VM) NAJA NAJA VENOM 280 ug in 1 mL Inactive Ingredients Ingredient Name Strength ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) ANHYDROUS TRISODIUM CITRATE (UNII: RS7A450LGA) METHYLPARABEN (UNII: A2I8C7HI9T) XYLITOL (UNII: VCQ006KQ1E) 2-(DIETHYLAMINO)ETHANOL (UNII: S6DL4M053U) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:47219-251-10 1 in 1 BOX 1 30 mL in 1 BOTTLE, SPRAY Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date Unapproved homeopathic 08/25/2009 Labeler - RECEPTOPHARM INC (145377888) Establishment Name Address ID/FEI Business Operations RECEPTOPHARM INC 145377888 ANALYSIS, MANUFACTURE, API MANUFACTURE Establishment Name Address ID/FEI Business Operations LIQUID PACKAGING RESOURCES 018935165 MANUFACTURE