Label: DRY MONTHSPRAY- dry month spray spray
- NDC Code(s): 84025-159-01
- Packager: Guangzhou Yanxi Biotechnology Co.. Ltd
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated August 18, 2024
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- DOSAGE & ADMINISTRATION
- WARNINGS
- INACTIVE INGREDIENT
- INDICATIONS & USAGE
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- PURPOSE
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
DRY MONTHSPRAY
dry month spray sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:84025-159 Route of Administration DENTAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN 5 mg in 100 mL XYLITOL (UNII: VCQ006KQ1E) (XYLITOL - UNII:VCQ006KQ1E) XYLITOL 3 mg in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Product Characteristics Color Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:84025-159-01 100 mL in 1 BOTTLE; Type 0: Not a Combination Product 08/19/2024 
Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M021 08/19/2024 Labeler - Guangzhou Yanxi Biotechnology Co.. Ltd (632583102) Establishment Name Address ID/FEI Business Operations Guangzhou Yanxi Biotechnology Co.. Ltd 632583102 manufacture(84025-159)
