USFDA APPLICATION NUMBER - 22113 / DOSAGE - TABLET;ORAL - 4MG;200MG;10MG
Active Ingredient/Active Moiety | ||
Ingredient Name | Basis of Strength | Strength |
---|---|---|
CHLORPHENIRAMINE MALEATE(UNII: V1Q0O9OJ9Z) (CHLORPHENIRAMINE - UNII:3U6IO1965U) | CHLORPHENIRAMINE MALEATE | 4mg | 4mg |
IBUPROFEN(UNII: WK2XYI10QM) (IBUPROFEN - UNII:WK2XYI10QM) | IBUPROFEN | 200mg | 200mg |
PHENYLEPHRINE HYDROCHLORIDE(UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV) | PHENYLEPHRINE HYDROCHLORIDE | 10mg | 10mg |
Inactive Ingredients
Ingredient Name | Haleon US Holdings LLC |
---|---|
ACESULFAME POTASSIUM(23OV73Q5G9) | |
CARNAUBA WAX(R12CBM0EIZ) | |
CROSCARMELLOSE SODIUM(M28OL1HH48) | |
EGG PHOSPHOLIPIDS(1Z74184RGV) | |
FERRIC OXIDE RED(1K09F3G675) | |
GLYCERIN(PDC6A3C0OX) | |
GLYCERYL DIBEHENATE(R8WTH25YS2) | |
HYPROMELLOSE, UNSPECIFIED(3NXW29V3WO) | |
LACTIC ACID, UNSPECIFIED FORM(33X04XA5AT) | |
LECITHIN, SOYBEAN(1DI56QDM62) | |
MALTODEXTRIN(7CVR7L4A2D) | |
MEDIUM-CHAIN TRIGLYCERIDES(C9H2L21V7U) | |
MICROCRYSTALLINE CELLULOSE(OP1R32D61U) | |
POLYDEXTROSE(VH2XOU12IE) | |
POLYVINYL ALCOHOL, UNSPECIFIED(532B59J990) | |
PROPYL GALLATE(8D4SNN7V92) | |
SILICON DIOXIDE(ETJ7Z6XBU4) | |
STARCH, CORN(O8232NY3SJ) | |
SUCRALOSE(96K6UQ3ZD4) | |
TALC(7SEV7J4R1U) | |
TITANIUM DIOXIDE(15FIX9V2JP) | |
TRIACETIN(XHX3C3X673) | |
XANTHAN GUM(TTV12P4NEE) |
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