Chillax is a Oral Spray in the Human Otc Drug category. It is labeled and distributed by Home Sweet Homeopathics. The primary component is Aconitum Napellus; Arsenic Acid; Bambusa Bambos Whole; Barium Carbonate; Calcium Carbonate; Calcium Phosphate; Hyoscyamus Niger; Strychnos Ignatii Seed; Lilium Lancifolium Whole Flowering; Lycopodium Clavatum Spore; Magnesium Chloride; Sodium Chloride; Sodium Sulfate; Strychnos Nux-vomica Seed; Phosphorus; Sepia Officinalis Juice; Silicon Dioxide; Delphinium Staphisagria Seed; Datura Stramonium.
Product ID | 59667-0034_686d297a-422b-4e7e-b669-cdb21a64ffa3 |
NDC | 59667-0034 |
Product Type | Human Otc Drug |
Proprietary Name | Chillax |
Generic Name | Aconite 30c, Arsenicum 30c, Bambusa 30c, Baryta Carb 30c, Calc Carb 30c, Calc Phos 30c, Hyoscyamus 30c, Ignatia 30c, Lilium Tig 30c, Lycopodium 30c, Mag Mur 30c, Nat Mur 30c,nat Sulph 30c, Nux Vomica 30c, Phosphorous 30c, Sepia 30c, Silicea 30c, Staphysagria 30c, Stramonium |
Dosage Form | Spray |
Route of Administration | ORAL |
Marketing Start Date | 2013-08-02 |
Marketing Category | UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC |
Labeler Name | Home Sweet Homeopathics |
Substance Name | ACONITUM NAPELLUS; ARSENIC ACID; BAMBUSA BAMBOS WHOLE; BARIUM CARBONATE; CALCIUM CARBONATE; CALCIUM PHOSPHATE; HYOSCYAMUS NIGER; STRYCHNOS IGNATII SEED; LILIUM LANCIFOLIUM WHOLE FLOWERING; LYCOPODIUM CLAVATUM SPORE; MAGNESIUM CHLORIDE; SODIUM CHLORIDE; SODIUM SULFATE; STRYCHNOS NUX-VOMICA SEED; PHOSPHORUS; SEPIA OFFICINALIS JUICE; SILICON DIOXIDE; DELPHINIUM STAPHISAGRIA SEED; DATURA STRAMONIUM |
Active Ingredient Strength | 30 [hp_C]/30[hp_C]; [hp_C]/30[hp_C]; [hp_C]/30[hp_C]; [hp_C]/30[hp_C]; [hp_C]/30[hp_C]; [hp_C]/30[hp_C]; [hp_C]/30[hp_C]; [hp_C]/30[hp_C]; [hp_C]/30[hp_C]; [hp_C]/30[hp_C]; [hp_C]/30[hp_C]; [hp_C]/30[hp_C]; [hp_C]/30[hp_C]; [hp_C]/30[hp_C]; [hp_C]/30[hp_C]; [hp_C]/30[hp_C]; [hp_C]/30[hp_C]; [hp_C]/30[hp_C]; [hp_C]/30[hp_C] |
NDC Exclude Flag | E |
Listing Certified Through | 2017-12-31 |
Marketing Start Date | 2013-08-02 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | unapproved homeopathic |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2013-08-02 |
Inactivation Date | 2019-11-27 |
Ingredient | Strength |
---|---|
ACONITUM NAPELLUS | 30 [hp_C]/30[hp_C] |