Allergies Total Mold Control: Homeopathic Product Information

ALLERGIES TOTAL MOLD CONTROL- arsenic trioxide, baptisia tinctoria root, chloramphenicol, echinacea, unspecified, elaeis guineensis fruit, goldenseal, mercurius solubilis, myrrh, nasturtium officinale, strychnos nux-vomica seed, phosphorus, phytolacca americana root, pulsatilla vulgaris, ricinus communis seed, sepia officinalis juice and zanthoxylum americanum bark 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 2 to 6 times daily until symptoms improve.

Adult Dose: 3 Pump Sprays

Child’s Dose (2-12): 2 Pump Sprays

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 allergy symptoms: •hypersensitivity •headache •sinus congestion •watery eyes •muscle/joint pain •temporary anxiety/depression •difficulty breathing •skin irritation

Active Ingredients: Arsenicum album, Baptisia tinctoria, Chloramphenicolum, Echinacea, Elaeis guineensis, Hydrastis canadensis, Mercurius solubilis, Myrrha, Nasturtium aquaticum, Nux vomica, Phosphorus, Phytolacca decandra, Pulsatilla, Ricinus communis, Sepia, Xanthoxylum fraxineum. ​Equal volumes of each ingredient in 12X, 24X, LM1 potencies.

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

Indications: For temporary relief of allergy symptoms:

  • hypersensitivity
  • headache
  • sinus congestion
  • watery eyes
  • muscle/joint pain
  • temporary anxiety/depression
  • difficulty breathing
  • skin irritation

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ALLERGIES TOTAL MOLD CONTROL
arsenicum album, baptisia tinctoria, chloramphenicolum, echinacea, elaeis guineensis, hydrastis canadensis, hydrastis canadensis, mercurius solubilis, myrrha, nasturtium aquaticum, nux vomica, phosphorus, phytolacca decandra, pulsatilla, ricinus communis, sepia, xanthoxylum fraxineum liquid
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:66579-0038
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ARSENIC TRIOXIDE (ARSENIC CATION (3+)) ARSENIC TRIOXIDE 12 [hp_X] in 29 mL
BAPTISIA TINCTORIA ROOT (BAPTISIA TINCTORIA ROOT) BAPTISIA TINCTORIA ROOT 12 [hp_X] in 29 mL
CHLORAMPHENICOL (CHLORAMPHENICOL) CHLORAMPHENICOL 12 [hp_X] in 29 mL
ECHINACEA, UNSPECIFIED (ECHINACEA, UNSPECIFIED) ECHINACEA, UNSPECIFIED 12 [hp_X] in 29 mL
ELAEIS GUINEENSIS FRUIT (ELAEIS GUINEENSIS FRUIT) ELAEIS GUINEENSIS FRUIT 12 [hp_X] in 29 mL
GOLDENSEAL (GOLDENSEAL) GOLDENSEAL 12 [hp_X] in 29 mL
MERCURIUS SOLUBILIS (MERCURIUS SOLUBILIS) MERCURIUS SOLUBILIS 12 [hp_X] in 29 mL
MYRRH (MYRRH) MYRRH 12 [hp_X] in 29 mL
NASTURTIUM OFFICINALE (NASTURTIUM AQUATICUM) NASTURTIUM OFFICINALE 12 [hp_X] in 29 mL
STRYCHNOS NUX-VOMICA SEED (STRYCHNOS NUX-VOMICA SEED) STRYCHNOS NUX-VOMICA SEED 12 [hp_X] in 29 mL
PHOSPHORUS (PHOSPHORUS) PHOSPHORUS 12 [hp_X] in 29 mL
PHYTOLACCA AMERICANA ROOT (PHYTOLACCA AMERICANA ROOT) PHYTOLACCA AMERICANA ROOT 12 [hp_X] in 29 mL
PULSATILLA VULGARIS (PULSATILLA VULGARIS) PULSATILLA VULGARIS 12 [hp_X] in 29 mL
RICINUS COMMUNIS SEED (RICINUS COMMUNIS SEED) RICINUS COMMUNIS SEED 12 [hp_X] in 29 mL
SEPIA OFFICINALIS JUICE (SEPIA OFFICINALIS JUICE) SEPIA OFFICINALIS JUICE 12 [hp_X] in 29 mL
ZANTHOXYLUM AMERICANUM BARK (ZANTHOXYLUM AMERICANUM BARK) ZANTHOXYLUM AMERICANUM BARK 12 [hp_X] in 29 mL
Inactive Ingredients
Ingredient Name Strength
CITRIC ACID MONOHYDRATE
POTASSIUM SORBATE
WATER
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:66579-0038-1 29 mL in 1 BOTTLE, SPRAY None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved homeopathic 08/05/2014
Labeler — New Sun Inc. (957251176)
Registrant — New Sun Inc. (957251176)

Revised: 08/2014 New Sun Inc.

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