Gout Symptom Reliever: Homeopathic Product Information

GOUT SYMPTOM RELIEVER- ammonium phosphate, dibasic, atropa belladonna, colchicum autumnale bulb, formic acid, fraxinus excelsior bark, fraxinus excelsior leaf, ledum palustre twig, sodium carbonate, strychnos nux-vomica seed and urtica urens liquid
New Sun Inc.

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.

Directions: Before initial dose depress pump 4-5 times or until primed and spray 1 dose directly in mouth 4 to 6 times daily until symptoms improve.

Adult Dose: 3 Pump Sprays

Child’s Dose (2-12): 2 Pump Sprays

Infants — 2 yrs. 1 Pump Spray

Warnings: If symptoms persist or worsen, seek advice of physician. If pregnant or breast-feeding, take only on advice of physician.

Keep out of reach of children.

Other information: Tamper resistant for your protection. Use only if safety seal is intact.

Indications: for temporary relief of pain in the:

  • great toe
  • heel
  • foot
  • joints

Including:

  • swelling
  • burning
  • itching
  • tingling
  • tearing pains
  • throbbing
  • cramps
  • shooting pains

Active Ingredients: Ammonium phosphoricum, Belladonna, Colchicum autumnale, Formicum acidum, Fraxinus excelsior, Ledum palustre, Natrum carbonicum, Nux vomica, urtica urens. ​Equal volumes of each ingredient in 10X, 30X, 100X potencies.

Inactive Ingredient: Citric acid, potassium sorbate, purified water.

Indications: For temporary relief of pain in the:

  • great toe
  • heel
  • foot
  • joints

Including:

  • swelling
  • burning
  • itching
  • tingling
  • tearing pains
  • throbbing
  • cramps
  • shooting pains

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GOUT SYMPTOM RELIEVER
ammonium phosphoricum, belladonna, colchicum autumnale, formicum acidum, fraxinus excelsior, ledum palustre, natrum carbonicum, nux vomica, urtica urens liquid
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:66579-0057
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
AMMONIUM PHOSPHATE, DIBASIC (PHOSPHATE ION) AMMONIUM PHOSPHATE, DIBASIC 10 [hp_X] in 59 mL
ATROPA BELLADONNA (ATROPA BELLADONNA) ATROPA BELLADONNA 10 [hp_X] in 59 mL
COLCHICUM AUTUMNALE BULB (COLCHICUM AUTUMNALE BULB) COLCHICUM AUTUMNALE BULB 10 [hp_X] in 59 mL
FORMIC ACID (FORMIC ACID) FORMIC ACID 10 [hp_X] in 59 mL
FRAXINUS EXCELSIOR BARK (FRAXINUS EXCELSIOR BARK) FRAXINUS EXCELSIOR BARK 10 [hp_X] in 59 mL
FRAXINUS EXCELSIOR LEAF (FRAXINUS EXCELSIOR LEAF) FRAXINUS EXCELSIOR LEAF 10 [hp_X] in 59 mL
LEDUM PALUSTRE TWIG (LEDUM PALUSTRE TWIG) LEDUM PALUSTRE TWIG 10 [hp_X] in 59 mL
SODIUM CARBONATE (CARBONATE ION) SODIUM CARBONATE 10 [hp_X] in 59 mL
STRYCHNOS NUX-VOMICA SEED (STRYCHNOS NUX-VOMICA SEED) STRYCHNOS NUX-VOMICA SEED 10 [hp_X] in 59 mL
URTICA URENS (URTICA URENS) URTICA URENS 10 [hp_X] in 59 mL
Inactive Ingredients
Ingredient Name Strength
CITRIC ACID MONOHYDRATE
POTASSIUM SORBATE
WATER
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:66579-0057-2 29 mL in 1 BOTTLE, SPRAY None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved homeopathic 08/29/2014
Labeler — New Sun Inc. (957251176)
Registrant — New Sun Inc. (957251176)

Revised: 08/2014 New Sun Inc.

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