NDC 59667-0101

Hand Foot Mouth

Antimonium Crudum 30c, Argentum Nit 30c, Borax 30c, Kali Chloricum 30c, Mercurius Corr 30c, Nat Mur 30c, Nitricum Ac 30c, Sulphuricum Acidum 30c

Hand Foot Mouth is a Oral Spray in the Human Otc Drug category. It is labeled and distributed by Home Sweet Homeopathics. The primary component is Antimony Trisulfide; Silver Nitrate; Sodium Borate; Potassium Chlorate; Mercuric Chloride; Sodium Chloride; Nitric Acid; Sulfuric Acid.

Product ID59667-0101_37edf4a0-9d71-450c-bf01-cd3641edb149
NDC59667-0101
Product TypeHuman Otc Drug
Proprietary NameHand Foot Mouth
Generic NameAntimonium Crudum 30c, Argentum Nit 30c, Borax 30c, Kali Chloricum 30c, Mercurius Corr 30c, Nat Mur 30c, Nitricum Ac 30c, Sulphuricum Acidum 30c
Dosage FormSpray
Route of AdministrationORAL
Marketing Start Date2013-08-02
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameHome Sweet Homeopathics
Substance NameANTIMONY TRISULFIDE; SILVER NITRATE; SODIUM BORATE; POTASSIUM CHLORATE; MERCURIC CHLORIDE; SODIUM CHLORIDE; NITRIC ACID; SULFURIC ACID
Active Ingredient Strength30 [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 FlagE
Listing Certified Through2017-12-31

Packaging

NDC 59667-0101-2

30 [hp_C] in 1 BOTTLE, SPRAY (59667-0101-2)
Marketing Start Date2013-08-02
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 59667-0101-2 [59667010102]

Hand Foot Mouth SPRAY
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2013-08-02
Inactivation Date2019-11-27

Drug Details

Active Ingredients

IngredientStrength
ANTIMONY TRISULFIDE30 [hp_C]/30[hp_C]

OpenFDA Data

SPL SET ID:5ab588e5-c2de-4077-a629-91a762f86af5
Manufacturer
UNII
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