Product NDC: | 67475-211 |
Proprietary Name: | Golden Sunshine Far Infrared Herbal |
Non Proprietary Name: | Topical Analgesic |
Active Ingredient(s): | .03; .03 g/g; g/g & nbsp; Topical Analgesic |
Administration Route(s): | TOPICAL |
Dosage Form(s): | PASTE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 67475-211 |
Labeler Name: | Golden Sunshine International, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part348 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20090223 |
Package NDC: | 67475-211-03 |
Package Description: | 450 g in 1 JAR (67475-211-03) |
NDC Code | 67475-211-03 |
Proprietary Name | Golden Sunshine Far Infrared Herbal |
Package Description | 450 g in 1 JAR (67475-211-03) |
Product NDC | 67475-211 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Topical Analgesic |
Dosage Form Name | PASTE |
Route Name | TOPICAL |
Start Marketing Date | 20090223 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Golden Sunshine International, Inc. |
Substance Name | MENTHOL; METHYL SALICYLATE |
Strength Number | .03; .03 |
Strength Unit | g/g; g/g |
Pharmaceutical Classes |