NDC 68703-122

AllergyEase Scent and Phenol

Acetaldehyde, Arsenicum Album, Balsamum Peruvianum, Calcarea Carbonica, Carbolicum Acidum, Conium, Coumarinum, Crocus Sativus, Histaminum Hydrochloricum, Lachesis, Lycopodium, Phosphorus, Sepia

AllergyEase Scent and Phenol is a Oral Spray in the Human Otc Drug category. It is labeled and distributed by Native Remedies, Llc. The primary component is Acetaldehyde; Arsenic Trioxide; Balsam Peru; Oyster Shell Calcium Carbonate, Crude; Phenol; Conium Maculatum Flowering Top; Coumarin; Saffron; Histamine Dihydrochloride; Lachesis Muta Venom; Lycopodium Clavatum Spore; Phosphorus; Sepia Officinalis Juice.

Product ID68703-122_c8284a2e-16a7-46bb-ba7a-4ef4362e5468
NDC68703-122
Product TypeHuman Otc Drug
Proprietary NameAllergyEase Scent and Phenol
Generic NameAcetaldehyde, Arsenicum Album, Balsamum Peruvianum, Calcarea Carbonica, Carbolicum Acidum, Conium, Coumarinum, Crocus Sativus, Histaminum Hydrochloricum, Lachesis, Lycopodium, Phosphorus, Sepia
Dosage FormSpray
Route of AdministrationORAL
Marketing Start Date2013-07-29
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameNative Remedies, LLC
Substance NameACETALDEHYDE; ARSENIC TRIOXIDE; BALSAM PERU; OYSTER SHELL CALCIUM CARBONATE, CRUDE; PHENOL; CONIUM MACULATUM FLOWERING TOP; COUMARIN; SAFFRON; HISTAMINE DIHYDROCHLORIDE; LACHESIS MUTA VENOM; LYCOPODIUM CLAVATUM SPORE; PHOSPHORUS; SEPIA OFFICINALIS JUICE
Active Ingredient Strength12 [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 68703-122-59

59 mL in 1 BOTTLE, GLASS (68703-122-59)
Marketing Start Date2013-07-29
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 68703-122-59 [68703012259]

AllergyEase Scent and Phenol SPRAY
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2013-07-29
Inactivation Date2020-01-31

Drug Details


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