| Product NDC: | 64272-736 |
| Proprietary Name: | AFRICAN SEA-COCONUT |
| Non Proprietary Name: | Elm |
| Active Ingredient(s): | 65 mg/5mL & nbsp; Elm |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SYRUP |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 64272-736 |
| Labeler Name: | LUEN FOOK MEDICINE SDN. BHD. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part356 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20120601 |
| Package NDC: | 64272-736-01 |
| Package Description: | 1 BOTTLE, GLASS in 1 BOX (64272-736-01) > 177 mL in 1 BOTTLE, GLASS |
| NDC Code | 64272-736-01 |
| Proprietary Name | AFRICAN SEA-COCONUT |
| Package Description | 1 BOTTLE, GLASS in 1 BOX (64272-736-01) > 177 mL in 1 BOTTLE, GLASS |
| Product NDC | 64272-736 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Elm |
| Dosage Form Name | SYRUP |
| Route Name | ORAL |
| Start Marketing Date | 20120601 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | LUEN FOOK MEDICINE SDN. BHD. |
| Substance Name | ELM |
| Strength Number | 65 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes |