Label: HY IQ WATER PET PRODUCT- hy iq water spray
- NDC Code(s): 76701-222-01, 76701-222-08
- Packager: HAND SANITIZER LLC
- Category: OTC ANIMAL DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.
Drug Label Information
Updated June 24, 2021
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- USES
- WARNINGS
- DIRECTIONS
- OTHER SAFETY INFORMATION
- INACTIVE INGREDIENTS
- HI IQ PET SPRAY
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INGREDIENTS AND APPEARANCE
HY IQ WATER PET PRODUCT
hy iq water sprayProduct Information Product Type OTC ANIMAL DRUG Item Code (Source) NDC:76701-222 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HYDROGEN CATION (UNII: 5046UKT60S) (HYDROGEN CATION - UNII:5046UKT60S) HYDROGEN CATION 10 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) 940 mg in 1 mL UREA (UNII: 8W8T17847W) 50 mg in 1 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:76701-222-01 50.275 mL in 1 BOTTLE, SPRAY 2 NDC:76701-222-08 237 mL in 1 BOTTLE, SPRAY Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 06/24/2021 Labeler - HAND SANITIZER LLC (117473019) Registrant - HAND SANITIZER LLC (117473019) Establishment Name Address ID/FEI Business Operations HAND SANITIZER LLC 117473019 api manufacture, manufacture, label