Product NDC: | 67777-402 |
Proprietary Name: | Saline Enema |
Non Proprietary Name: | SALINE ENEMA |
Active Ingredient(s): | 7; 19 g/118mL; g/118mL & nbsp; SALINE ENEMA |
Administration Route(s): | RECTAL |
Dosage Form(s): | ENEMA |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 67777-402 |
Labeler Name: | Dynarex Corporation |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part334 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20120829 |
Package NDC: | 67777-402-01 |
Package Description: | 48 BOX in 1 CASE (67777-402-01) > 1 BOTTLE in 1 BOX > 118 mL in 1 BOTTLE |
NDC Code | 67777-402-01 |
Proprietary Name | Saline Enema |
Package Description | 48 BOX in 1 CASE (67777-402-01) > 1 BOTTLE in 1 BOX > 118 mL in 1 BOTTLE |
Product NDC | 67777-402 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | SALINE ENEMA |
Dosage Form Name | ENEMA |
Route Name | RECTAL |
Start Marketing Date | 20120829 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Dynarex Corporation |
Substance Name | SODIUM PHOSPHATE, DIBASIC; SODIUM PHOSPHATE, MONOBASIC |
Strength Number | 7; 19 |
Strength Unit | g/118mL; g/118mL |
Pharmaceutical Classes |