Label: HY-IQ SANITIZER AND DISINFECTANT- hy-iq water spray
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Contains inactivated NDC Code(s)
NDC Code(s): 76701-360-22 - Packager: HAND SANITIZER LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated June 23, 2021
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- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
- OTHER SAFETY INFORMATION
- INACTIVE INGREDIENT
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
HY-IQ SANITIZER AND DISINFECTANT
hy-iq water sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:76701-360 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 UREA (UNII: 8W8T17847W) 50 mg in 1 mL WATER (UNII: 059QF0KO0R) 940 mg in 1 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:76701-360-22 1.7 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 06/21/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 06/21/2021 Labeler - HAND SANITIZER LLC (117473019) Establishment Name Address ID/FEI Business Operations HAND SANITIZER LLC 117473019 manufacture(76701-360) , label(76701-360) , pack(76701-360)