Label: FEXOFENADINE HCL tablet
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NDC Code(s):
71205-531-10,
71205-531-15,
71205-531-20,
71205-531-30, view more71205-531-60, 71205-531-90
- Packager: Proficient Rx LP
- This is a repackaged label.
- Source NDC Code(s): 69230-300
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated March 1, 2024
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT(S), in each tablet
- PURPOSE
- USE(S)
- WARNINGS
- DO NOT USE
- ASK A DOCTOR BEFORE USE IF
- WHEN USING THIS PRODUCT
- STOP USE AND ASK A DOCTOR IF
- KEEP OUT OF REACH OF CHILDREN
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DIRECTIONS
60 mg
adults and children 12 years of age and over
take one 60 mg tablet with water every 12 hours; do not take more than 2 tablets in 24 hours
children under 12 years of age
do not use
adults 65 years of age and older
ask a doctor
consumers with kidney disease
ask a doctor
180 mg
adults and children 12 years of age and over
take one 180 mg tablet with water once a day; do not take more than 1 tablet in 24 hours
children under 12 years of age
do not use
adults 65 years of age and older
ask a doctor
consumers with kidney disease
ask a doctor
- OTHER INFORMATION
- INACTIVE INGREDIENTS
- QUESTIONS OR COMMENTS
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
FEXOFENADINE HCL
fexofenadine hcl tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71205-531(NDC:69230-300) Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength FEXOFENADINE HYDROCHLORIDE (UNII: 2S068B75ZU) (FEXOFENADINE - UNII:E6582LOH6V) FEXOFENADINE HYDROCHLORIDE 180 mg Inactive Ingredients Ingredient Name Strength SILICON DIOXIDE (UNII: ETJ7Z6XBU4) HYPROMELLOSE 2910 (6 MPA.S) (UNII: 0WZ8WG20P6) LIGHT MINERAL OIL (UNII: N6K5787QVP) MAGNESIUM STEARATE (UNII: 70097M6I30) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) POLYSORBATE 80 (UNII: 6OZP39ZG8H) STARCH, CORN (UNII: O8232NY3SJ) FERRIC OXIDE RED (UNII: 1K09F3G675) FERRIC OXIDE YELLOW (UNII: EX438O2MRT) SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2) TALC (UNII: 7SEV7J4R1U) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) POLYETHYLENE GLYCOL 6000 (UNII: 30IQX730WE) Product Characteristics Color PINK Score no score Shape CAPSULE Size 18mm Flavor Imprint Code J;44 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71205-531-10 10 in 1 BOTTLE; Type 0: Not a Combination Product 03/11/2024 2 NDC:71205-531-15 15 in 1 BOTTLE; Type 0: Not a Combination Product 03/11/2024 3 NDC:71205-531-20 20 in 1 BOTTLE; Type 0: Not a Combination Product 03/11/2024 4 NDC:71205-531-30 30 in 1 BOTTLE; Type 0: Not a Combination Product 02/03/2021 5 NDC:71205-531-60 60 in 1 BOTTLE; Type 0: Not a Combination Product 02/03/2021 6 NDC:71205-531-90 90 in 1 BOTTLE; Type 0: Not a Combination Product 02/03/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA204097 08/19/2016 Labeler - Proficient Rx LP (079196022) Establishment Name Address ID/FEI Business Operations Proficient Rx LP 079196022 REPACK(71205-531) , RELABEL(71205-531)