Label: HYDRATING MOUTHSPRAY liquid
- NDC Code(s): 84025-251-01
- Packager: Guangzhou Yanxi Biotechnology Co., Ltd
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated November 8, 2024
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- DOSAGE & ADMINISTRATION
- WARNINGS
- INACTIVE INGREDIENT
- INDICATIONS & USAGE
- KEEP OUT OF REACH OF CHILDREN
- PURPOSE
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
HYDRATING MOUTHSPRAY
hydrating mouthspray liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:84025-251 Route of Administration CUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 2 mg in 50 mL XYLITOL (UNII: VCQ006KQ1E) (XYLITOL - UNII:VCQ006KQ1E) XYLITOL 3 mg in 50 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:84025-251-01 50 mL in 1 BOTTLE; Type 0: Not a Combination Product 11/08/2024 
Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M026 11/08/2024 Labeler - Guangzhou Yanxi Biotechnology Co., Ltd (632583102) Establishment Name Address ID/FEI Business Operations Guangzhou Yanxi Biotechnology Co., Ltd 632583102 manufacture(84025-251)
