Product NDC: | 0713-0535 |
Proprietary Name: | Formulation R |
Non Proprietary Name: | Phenylephrine Hydrochloride, Hydrogenate Palm Kernel Oil |
Active Ingredient(s): | 855; 2.5 mg/1; mg/1 & nbsp; Phenylephrine Hydrochloride, Hydrogenate Palm Kernel Oil |
Administration Route(s): | RECTAL |
Dosage Form(s): | SUPPOSITORY |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0713-0535 |
Labeler Name: | G&W Laboratories, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part346 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20020624 |
Package NDC: | 0713-0535-24 |
Package Description: | 24 SUPPOSITORY in 1 CARTON (0713-0535-24) |
NDC Code | 0713-0535-24 |
Proprietary Name | Formulation R |
Package Description | 24 SUPPOSITORY in 1 CARTON (0713-0535-24) |
Product NDC | 0713-0535 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Phenylephrine Hydrochloride, Hydrogenate Palm Kernel Oil |
Dosage Form Name | SUPPOSITORY |
Route Name | RECTAL |
Start Marketing Date | 20020624 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | G&W Laboratories, Inc. |
Substance Name | HYDROGENATED PALM KERNEL OIL; PHENYLEPHRINE HYDROCHLORIDE |
Strength Number | 855; 2.5 |
Strength Unit | mg/1; mg/1 |
Pharmaceutical Classes |