| Product NDC: | 62699-1114 |
| Proprietary Name: | Golden Sunshine Herbal |
| Non Proprietary Name: | Topical Analgesic |
| Active Ingredient(s): | .00781; .03 g/g; g/g & nbsp; Topical Analgesic |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SPRAY |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 62699-1114 |
| Labeler Name: | Nan Mei Pharmaceutical Co., Ltd. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20040802 |
| Package NDC: | 62699-1114-1 |
| Package Description: | 20 BOX in 1 BOX (62699-1114-1) > 1 CAN in 1 BOX > 105 g in 1 CAN |
| NDC Code | 62699-1114-1 |
| Proprietary Name | Golden Sunshine Herbal |
| Package Description | 20 BOX in 1 BOX (62699-1114-1) > 1 CAN in 1 BOX > 105 g in 1 CAN |
| Product NDC | 62699-1114 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Topical Analgesic |
| Dosage Form Name | SPRAY |
| Route Name | TOPICAL |
| Start Marketing Date | 20040802 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Nan Mei Pharmaceutical Co., Ltd. |
| Substance Name | MENTHOL; METHYL SALICYLATE |
| Strength Number | .00781; .03 |
| Strength Unit | g/g; g/g |
| Pharmaceutical Classes |