Label: THERAFLEX GLUCOSAMINE PLUS MAX- d-glucosamine hydrochloride, chondroitin sulfate sodium1 capsule
- NDC Code(s): 61841-055-12, 61841-055-30, 61841-055-60
- Packager: Bayer HealthCare LLC.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Export only
Drug Label Information
Updated January 10, 2024
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- Official Label (Printer Friendly)
- Drug Facts
- ACTIVE INGREDIENT
- INDICATIONS & USAGE
- WARNINGS
- DO NOT USE
- ASK DOCTOR
- ASK DOCTOR/PHARMACIST
- WHEN USING
- STOP USE
- PREGNANCY OR BREAST FEEDING
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
- OTHER SAFETY INFORMATION
- INACTIVE INGREDIENT
- QUESTIONS
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
THERAFLEX GLUCOSAMINE PLUS MAX
d-glucosamine hydrochloride, chondroitin sulfate sodium1 capsuleProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:61841-055 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CHONDROITIN SULFATE SODIUM (BOVINE) (UNII: 8QTV3DTT8W) (CHONDROITIN SULFATE (BOVINE) - UNII:6IC1M3OG5Z) CHONDROITIN SULFATE (BOVINE) 500 mg Inactive Ingredients Ingredient Name Strength MANGANESE SULFATE (UNII: W00LYS4T26) Product Characteristics Color white Score no score Shape OVAL Size 18mm Flavor Imprint Code ; Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:61841-055-12 1 in 1 CARTON 07/01/2015 1 120 in 1 BOTTLE; Type 0: Not a Combination Product 2 NDC:61841-055-60 1 in 1 CARTON 07/01/2015 2 60 in 1 BOTTLE; Type 0: Not a Combination Product 3 NDC:61841-055-30 1 in 1 CARTON 07/01/2015 3 30 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 07/01/2015 Labeler - Bayer HealthCare LLC. (785159372)
