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Golden Sunshine Herbal
Golden Sunshine Herbal - 67475-114-03 - (Topical Analgesic)
Drug Information of Golden Sunshine Herbal
| Product NDC: | 67475-114 |
| 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) |
Labeler Information of Golden Sunshine Herbal
| Product NDC: | 67475-114 |
| Labeler Name: | Golden Sunshine International, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20040802 |
Package Information of Golden Sunshine Herbal
| Package NDC: | 67475-114-03 |
| Package Description: | 7 g in 1 VIAL (67475-114-03) |
NDC Information of Golden Sunshine Herbal
| NDC Code | 67475-114-03 |
| Proprietary Name | Golden Sunshine Herbal |
| Package Description | 7 g in 1 VIAL (67475-114-03) |
| Product NDC | 67475-114 |
| 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 | Golden Sunshine International, Inc. |
| Substance Name | MENTHOL; METHYL SALICYLATE |
| Strength Number | .00781; .03 |
| Strength Unit | g/g; g/g |
| Pharmaceutical Classes |
