| Product NDC: | 53799-601 |
| Proprietary Name: | Sleeplessness Relief |
| Non Proprietary Name: | Avena sativa and Hepar sulphuris and Pulsatilla and Zincum valerianicum |
| Active Ingredient(s): | 12; 12; 15; 12 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1 & nbsp; Avena sativa and Hepar sulphuris and Pulsatilla and Zincum valerianicum |
| Administration Route(s): | ORAL |
| Dosage Form(s): | GLOBULE |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 53799-601 |
| Labeler Name: | Similasan AG |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20090101 |
| Package NDC: | 53799-601-30 |
| Package Description: | 1078 GLOBULE in 1 BOTTLE, GLASS (53799-601-30) |
| NDC Code | 53799-601-30 |
| Proprietary Name | Sleeplessness Relief |
| Package Description | 1078 GLOBULE in 1 BOTTLE, GLASS (53799-601-30) |
| Product NDC | 53799-601 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Avena sativa and Hepar sulphuris and Pulsatilla and Zincum valerianicum |
| Dosage Form Name | GLOBULE |
| Route Name | ORAL |
| Start Marketing Date | 20090101 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | Similasan AG |
| Substance Name | AVENA SATIVA FLOWERING TOP; CALCIUM SULFIDE; PULSATILLA PATENS; ZINC VALERATE DIHYDRATE |
| Strength Number | 12; 12; 15; 12 |
| Strength Unit | [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1 |
| Pharmaceutical Classes |