 
				 
										
USFDA APPLICATION NUMBER - 21394 / DOSAGE - TABLET;ORAL - 38MG;200MG
| Active Ingredient/Active Moiety | ||
| Ingredient Name | Basis of Strength | Strength | 
|---|---|---|
| DIPHENHYDRAMINE CITRATE(UNII: 4OD433S209) (DIPHENHYDRAMINE - UNII:8GTS82S83M) | DIPHENHYDRAMINE CITRATE | 38mg | 
| IBUPROFEN(UNII: WK2XYI10QM) (IBUPROFEN - UNII:WK2XYI10QM) | IBUPROFEN | 200mg | 
Inactive Ingredients