Label: THERAFLEX ADVANCE (ibuprofen, glucosamine sulfate, and chondroitin sulfate- bovine tablet
- NDC Code(s): 61841-152-12, 61841-152-72
- Packager: Bayer HealthCare LLC.
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated January 10, 2024
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENT
- Uses
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Warnings
Allergy alert
Ibuprofen may cause a severe allergic reaction wich may include:
- hives
- facial swelling
- asthma (wheezing)
- shock.
Alcohol warning
If you consume 3 or more alcoholic drinks every day, ask your doctor whether you should take ibuprofen or other pain relieves/fever reducers. Ibuprofen may cause stomach bleeding.
- Directions
- Other information
- Inactive ingredients
- PRINCIPAL DISPLAY PANEL - 60 Capsule Bottle Carton
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INGREDIENTS AND APPEARANCE
THERAFLEX ADVANCE
ibuprofen, glucosamine sulfate, and chondroitin sulfate (bovine) tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:61841-152 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength IBUPROFEN (UNII: WK2XYI10QM) (IBUPROFEN - UNII:WK2XYI10QM) IBUPROFEN 100 mg GLUCOSAMINE SULFATE (UNII: 1FW7WLR731) (GLUCOSAMINE - UNII:N08U5BOQ1K) GLUCOSAMINE SULFATE 250 mg CHONDROITIN SULFATE (BOVINE) (UNII: 6IC1M3OG5Z) (CONDOLIASE - UNII:7SI2UZG934) CHONDROITIN SULFATE (BOVINE) 200 mg Inactive Ingredients Ingredient Name Strength STARCH, CORN (UNII: O8232NY3SJ) CROSPOVIDONE (UNII: 68401960MK) GELATIN (UNII: 2G86QN327L) MAGNESIUM STEARATE (UNII: 70097M6I30) CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) STEARIC ACID (UNII: 4ELV7Z65AP) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) Product Characteristics Color blue (Blue opaque) Score no score Shape OVAL Size 22mm Flavor Imprint Code Theraflex;Advance Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:61841-152-72 1 in 1 CARTON 12/11/2014 1 60 in 1 BOTTLE; Type 0: Not a Combination Product 2 NDC:61841-152-12 1 in 1 CARTON 12/11/2014 2 120 in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date Export only 12/11/2014 Labeler - Bayer HealthCare LLC. (785159372)