Label: SKIN AND ITCH- pulex i., rhus tox., staphysagria, sulphur, urtica, graphites liquid
- NDC Code(s): 61571-548-15
- Packager: HomeoPet, LLC
- Category: OTC ANIMAL DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved homeopathic
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Drug Label Information
Updated October 30, 2020
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Directions for Use and Dosage
DIRECTIONS FOR USE:
- Dose remedy directly into mouth, in water or at meal/snack time
- Administer one dose 3 times per day, as needed
- In acute cases, one dose every 15 minutes up to 4 doses may be given
- When improvement is seen decrease frequency of dosing to twice daily, then once daily. If symptoms reappear repeat original dose. Discontinue use when symptoms subside
DOSAGE weight (lb)
drops per dose
animals less than 1 lb
2 in at least 8 oz of water
1-20
5
21-60
10
61-100
15
over 100
20
- Contact Veterinarian
- Ingredients HPUS: Active
- Inactive Ingredients
- Skin & Itch
- Indications
- Skin and Itch box
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INGREDIENTS AND APPEARANCE
SKIN AND ITCH
pulex i., rhus tox., staphysagria, sulphur, urtica, graphites liquidProduct Information Product Type OTC ANIMAL DRUG Item Code (Source) NDC:61571-548 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength GRAPHITE (UNII: 4QQN74LH4O) (GRAPHITE - UNII:4QQN74LH4O) GRAPHITE 6 [hp_C] in 15 mL PULEX IRRITANS (UNII: L63DD62R8R) (PULEX IRRITANS - UNII:L63DD62R8R) PULEX IRRITANS 6 [hp_C] in 15 mL TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (TOXICODENDRON PUBESCENS LEAF - UNII:6IO182RP7A) TOXICODENDRON PUBESCENS LEAF 6 [hp_C] in 15 mL DELPHINIUM STAPHISAGRIA SEED (UNII: 00543AP1JV) (DELPHINIUM STAPHISAGRIA SEED - UNII:00543AP1JV) DELPHINIUM STAPHISAGRIA SEED 6 [hp_C] in 15 mL SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70) SULFUR 6 [hp_C] in 15 mL URTICA DIOICA (UNII: 710FLW4U46) (URTICA DIOICA - UNII:710FLW4U46) URTICA DIOICA 6 [hp_C] in 15 mL Inactive Ingredients Ingredient Name Strength ALCOHOL (UNII: 3K9958V90M) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:61571-548-15 15 mL in 1 BOTTLE, DROPPER Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 09/20/1999 Labeler - HomeoPet, LLC (121272657) Registrant - HomeoPet, LLC (121272657) Establishment Name Address ID/FEI Business Operations Speciality Pharma Manufacturing LLC 013957125 api manufacture, manufacture