Label: PAIN RELIEF MENTHOL AND SNAKE VENOM (cobra venom (naja naja) 2x, menthol (mentholum) tinc, moccasin venom- a.piscivorus 4x gel
- NDC Code(s): 73002-142-02
- 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 December 27, 2023
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- Official Label (Printer Friendly)
- Active Ingredients Purpose
- PURPOSE
- Indication:
- KEEP OUT OF REACH OF CHILDREN
-
Warnings:
• For external use only.Not for use on open wounds.
• If symptoms persist or worsen, discontinue use, seek medical attention.
• Avoid contact with eyes. If product gets into eyes, flush with water, seek medical attention.
• If rash, redness, irritation or itching occurs, discontinue use.
• If pregnant or breastfeeding ask a health professional before use.
• If swallowed, get medical help or contact a Poison Center.
• Keep out of reach of children. -
Directions For Use:
- Liberally apply gel to affected area and rub into joints.
- Use 3-4 times per day for the first week. Use as needed thereafter to relieve discomfort.
- Use no more than 4 times per day.
- 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 MENTHOL AND SNAKE VENOM
cobra venom (naja naja) 2x, menthol (mentholum) tinc, moccasin venom (a.piscivorus) 4x gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73002-142 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 0.1 mg in 1 mL MENTHOL, (+)- (UNII: C6B1OE8P3W) (MENTHOL, (+)- - UNII:C6B1OE8P3W) MENTHOL, (+)- 1 mg in 1 mL AGKISTRODON PISCIVORUS VENOM (UNII: X9V1Q8U150) (AGKISTRODON PISCIVORUS VENOM - UNII:X9V1Q8U150) AGKISTRODON PISCIVORUS VENOM 0.001 mg in 1 mL Inactive Ingredients Ingredient Name Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) GLYCERIN (UNII: PDC6A3C0OX) HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) WATER (UNII: 059QF0KO0R) SODIUM CHLORIDE (UNII: 451W47IQ8X) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73002-142-02 56 mL in 1 BOTTLE; 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)