Label: SUN WAVE CONSUMER ANTISEPTIC HAND SANITIZER- isopropyl alcohol spray
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Contains inactivated NDC Code(s)
NDC Code(s): 75023-001-01 - Packager: SUN WAVE WELLNESS, LLC
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated April 10, 2020
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- Inactive ingredients
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
SUN WAVE CONSUMER ANTISEPTIC HAND SANITIZER
isopropyl alcohol sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:75023-001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL 70 mL in 100 mL Inactive Ingredients Ingredient Name Strength LIMONENE, (+)- (UNII: GFD7C86Q1W) 1 mL in 100 mL GLYCERIN (UNII: PDC6A3C0OX) 2 mL in 100 mL ALOE VERA LEAF (UNII: ZY81Z83H0X) 1 mL in 100 mL WATER (UNII: 059QF0KO0R) 26 mL in 100 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:75023-001-01 100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 04/30/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 04/30/2020 Labeler - SUN WAVE WELLNESS, LLC (117465590) Registrant - SUN WAVE WELLNESS, LLC (117465590) Establishment Name Address ID/FEI Business Operations SUN WAVE WELLNESS LLC 117465590 manufacture(75023-001)