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USFDA APPLICATION NUMBER - 21374 / DOSAGE - CAPSULE;ORAL - EQ 200MG FREE ACID AND POTASSIUM SALT;30MG
| Active Ingredient/Active Moiety | ||
| Ingredient Name | Basis of Strength | Strength |
|---|---|---|
| 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 |
|---|---|
| D&C YELLOW NO. 10(35SW5USQ3G) | |
| FD&C RED NO. 40(WZB9127XOA) | |
| GELATIN, UNSPECIFIED(2G86QN327L) | |
| MEDIUM-CHAIN TRIGLYCERIDES(C9H2L21V7U) | |
| POLYETHYLENE GLYCOL, UNSPECIFIED(3WJQ0SDW1A) | |
| POTASSIUM HYDROXIDE(WZH3C48M4T) | |
| SORBITAN(6O92ICV9RU) | |
| SORBITOL(506T60A25R) | |
| WATER(059QF0KO0R) |
