- Active Ingredients
- Purpose
- Uses:
- Warnings:
- KEEP OUT OF REACH OF CHILDREN
- Directions for Use:
-
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 severe (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
-
INGREDIENTS AND APPEARANCE
NYLOXIN
naja naja venom gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:47219-311 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:47219-311-02 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)