Label: NYLOXIN- naja naja venom gel
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Contains inactivated NDC Code(s)
NDC Code(s): 47219-301-02 - Packager: Nutra Pharma Corporation
- 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 July 14, 2021
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- Active Ingredients
- Purpose
- Uses:
- Warnings:
- KEEP OUT OF REACH OF CHILDREN
- Directions for Use:
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Other Information:
- Do not use if container seal is broken prior to opening.
- This product is intended for use in cases of recurring joint pain.
- This product is NOT intended to treat disease, it provides a temporary level of comfort, relief and a feeling of wellness.
- This product has been determined to be safe and effective for moderate to sever (Stage 2) chronic pain, as indicated by the Homeopathic Pharmacopeia of the United States.
- Do not use if container seal is broken prior to opening.
- ASK DOCTOR
- Inactive Ingredients:
- QUESTIONS
- Product label
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INGREDIENTS AND APPEARANCE
NYLOXIN
naja naja venom gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:47219-301 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NAJA NAJA VENOM (UNII: ZZ4AG7L7VM) (NAJA NAJA VENOM - UNII:ZZ4AG7L7VM) NAJA NAJA VENOM 4 [hp_X] in 1 mL Inactive Ingredients Ingredient Name Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) ALCOHOL (UNII: 3K9958V90M) HYDROXYPROPYL CELLULOSE (UNII: RFW2ET671P) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) SODIUM CHLORIDE (UNII: 451W47IQ8X) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:47219-301-02 1 in 1 BOX 08/23/2010 1 60 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 08/23/2010 Labeler - Nutra Pharma Corporation (141236286)