Product NDC: | 37808-678 |
Proprietary Name: | hemorrhoidal |
Non Proprietary Name: | Mineral oil, petrolatum, phenylephrine hcl |
Active Ingredient(s): | 140; 719; 2.5 mg/100g; mg/100g; mg/100g & nbsp; Mineral oil, petrolatum, phenylephrine hcl |
Administration Route(s): | RECTAL |
Dosage Form(s): | OINTMENT |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 37808-678 |
Labeler Name: | H E B |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part346 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20121216 |
Package NDC: | 37808-678-16 |
Package Description: | 1 TUBE in 1 CARTON (37808-678-16) > 57 g in 1 TUBE |
NDC Code | 37808-678-16 |
Proprietary Name | hemorrhoidal |
Package Description | 1 TUBE in 1 CARTON (37808-678-16) > 57 g in 1 TUBE |
Product NDC | 37808-678 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Mineral oil, petrolatum, phenylephrine hcl |
Dosage Form Name | OINTMENT |
Route Name | RECTAL |
Start Marketing Date | 20121216 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | H E B |
Substance Name | MINERAL OIL; PETROLATUM; PHENYLEPHRINE HYDROCHLORIDE |
Strength Number | 140; 719; 2.5 |
Strength Unit | mg/100g; mg/100g; mg/100g |
Pharmaceutical Classes |