USFDA APPLICATION NUMBER - 21441 / DOSAGE - TABLET;ORAL - 2MG;200MG;30MG
Active Ingredient/Active Moiety | ||
Ingredient Name | Basis of Strength | Strength |
---|---|---|
CHLORPHENIRAMINE MALEATE(UNII: V1Q0O9OJ9Z) (CHLORPHENIRAMINE - UNII:3U6IO1965U) | CHLORPHENIRAMINE MALEATE | 2mg |
IBUPROFEN(UNII: WK2XYI10QM) (IBUPROFEN - UNII:WK2XYI10QM) | IBUPROFEN | 200mg |
PSEUDOEPHEDRINE HYDROCHLORIDE(UNII: 6V9V2RYJ8N) (PSEUDOEPHEDRINE - UNII:7CUC9DDI9F) | PSEUDOEPHEDRINE HYDROCHLORIDE | 30mg |
Inactive Ingredients
Ingredient Name | Haleon US Holdings LLC |
---|---|
CARNAUBA WAX(R12CBM0EIZ) | |
CROSCARMELLOSE SODIUM(M28OL1HH48) | |
FD&C RED NO. 40(WZB9127XOA) | |
FD&C YELLOW NO. 6(H77VEI93A8) | |
GLYCERYL DIBEHENATE(R8WTH25YS2) | |
HYPROMELLOSE, UNSPECIFIED(3NXW29V3WO) | |
MICROCRYSTALLINE CELLULOSE(OP1R32D61U) | |
POLYDEXTROSE(VH2XOU12IE) | |
POLYETHYLENE GLYCOL, UNSPECIFIED(3WJQ0SDW1A) | |
SILICON DIOXIDE(ETJ7Z6XBU4) | |
STARCH, CORN(O8232NY3SJ) | |
TITANIUM DIOXIDE(15FIX9V2JP) |
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