Label: DRI-EAR suspension/ drops
- NDC Code(s): 12258-153-01
- Packager: S.S.S. Company
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated March 5, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Doasge and Administration.
- Warnings
- Inactive Ingredient
- Indication
- KEEP OUT OF REACH OF CHILDREN
- Purpose
- Dri-Ear Carton
-
INGREDIENTS AND APPEARANCE
DRI-EAR
dri-ear suspension/ dropsProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:12258-153 Route of Administration AURICULAR (OTIC) Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL 950 mg in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:12258-153-01 30 mL in 1 BOTTLE; Type 0: Not a Combination Product 04/30/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M014 04/30/2024 Labeler - S.S.S. Company (003288321) Registrant - S.S.S. Company (003288321) Establishment Name Address ID/FEI Business Operations S.S.S. Company 003288321 manufacture(12258-153)
