Product NDC: | 52471-111 |
Proprietary Name: | Sorbitol |
Non Proprietary Name: | Sorbitol |
Active Ingredient(s): | 1 g/mL & nbsp; Sorbitol |
Administration Route(s): | RECTAL |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 52471-111 |
Labeler Name: | H&H Laboratories, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part334 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20130610 |
Package NDC: | 52471-111-16 |
Package Description: | 473 mL in 1 BOTTLE (52471-111-16) |
NDC Code | 52471-111-16 |
Proprietary Name | Sorbitol |
Package Description | 473 mL in 1 BOTTLE (52471-111-16) |
Product NDC | 52471-111 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Sorbitol |
Dosage Form Name | SOLUTION |
Route Name | RECTAL |
Start Marketing Date | 20130610 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | H&H Laboratories, Inc. |
Substance Name | SORBITOL |
Strength Number | 1 |
Strength Unit | g/mL |
Pharmaceutical Classes |