Label: QPR QUICK PAIN RELIEF- naja naja venom gel
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Contains inactivated NDC Code(s)
NDC Code(s): 47219-341-02 - Packager: Nutra Pharma Corporation
- This is a repackaged label.
- Source NDC Code(s): 47219-301
- 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 September 22, 2016
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active Ingredients
- Purpose
- Uses
- Warnings
- Directions For Use
- KEEP OUT OF REACH OF CHILDREN
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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 severe (Stage 2) chronic pain, as indicated by the Homeopathic Pharmacopeia of the United States.
- Pregnant or nursing women and children should consult a physician before use.
- Inactive Ingredients
- Questions?
- PRINCIPAL DISPLAY PANEL - 60 mL Bottle Label
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INGREDIENTS AND APPEARANCE
QPR QUICK PAIN RELIEF
naja naja venom gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:47219-341(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) Propylene Glycol (UNII: 6DC9Q167V3) Sodium Chloride (UNII: 451W47IQ8X) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:47219-341-02 60 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product 09/15/2016 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date UNAPPROVED HOMEOPATHIC 09/15/2016 Labeler - Nutra Pharma Corporation (141236286) Establishment Name Address ID/FEI Business Operations Receptopharm, Inc 145377888 API MANUFACTURE(47219-341) , REPACK(47219-341) , RELABEL(47219-341)