Label: PAIN RELIEF CAFFEINE AND SNAKE VENOM (caffeine (coffeinum) 6x, cobra venom (naja naja) 5x, moccasin venom- a.piscivorus 7x spray
- NDC Code(s): 73002-131-01
- Packager: Green Earth Health 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 1, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredients Purpose
- PURPOSE
- Indication:
- KEEP OUT OF REACH OF CHILDREN
-
Warnings:
• Side effects might include headache, nausea, sore throat, allergic rhinitis, gastrointestinal discomfort, itchiness or mild rash.
• Limit the use of caffeine-containing medications, foods, or beverages while taking this product because too much caffeine may cause nervousness, irritability, sleeplessness, and, occasionally, rapid heart beat.
• If symptoms persist or worsen, stop using this product and consult physician.
• Avoid contact with eyes. If product gets into eyes, flush with water. Seek medical attention.
• If pregnant or breastfeeding ask a health professional before use.
• Keep out of reach of children. -
Directions For Use:
- Do not use if tamper-proof cover is damaged.
- Press down 4 times to prime the pump.
- Spray 2 times directly into the mouth or under the tongue.
- Start using 3 times per day. Use as needed thereafter to relieve discomfort.
- Allow several days for product to take maximum effect.
- Use within 60 days from opening. Store at 50° to 75°F (10°C to 24°C)
- Inactive Ingredients:
- Product label
-
INGREDIENTS AND APPEARANCE
PAIN RELIEF CAFFEINE AND SNAKE VENOM
caffeine (coffeinum) 6x, cobra venom (naja naja) 5x, moccasin venom (a.piscivorus) 7x sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73002-131 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CAFFEINE (UNII: 3G6A5W338E) (CAFFEINE - UNII:3G6A5W338E) CAFFEINE 6 [hp_X] in 1 mL NAJA NAJA VENOM (UNII: ZZ4AG7L7VM) (NAJA NAJA VENOM - UNII:ZZ4AG7L7VM) NAJA NAJA VENOM 4 [hp_X] in 1 mL AGKISTRODON PISCIVORUS VENOM (UNII: X9V1Q8U150) (AGKISTRODON PISCIVORUS VENOM - UNII:X9V1Q8U150) AGKISTRODON PISCIVORUS VENOM 6 [hp_X] in 1 mL Inactive Ingredients Ingredient Name Strength ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) WATER (UNII: 059QF0KO0R) SODIUM BENZOATE (UNII: OJ245FE5EU) SODIUM PHOSPHATE, MONOBASIC, ANHYDROUS (UNII: KH7I04HPUU) XYLITOL (UNII: VCQ006KQ1E) VANILLA (UNII: Q74T35078H) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73002-131-01 28 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 09/01/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 09/01/2020 Labeler - Green Earth Health Inc. (116983264) Registrant - Green Earth Health Inc. (116983264)
