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Naturasil
Naturasil - 10893-625-30 - (Sulfur)
Drug Information of Naturasil
| Product NDC: | 10893-625 |
| Proprietary Name: | Naturasil |
| Non Proprietary Name: | Sulfur |
| Active Ingredient(s): | 6 [hp_X]/1 & nbsp; Sulfur |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Naturasil
| Product NDC: | 10893-625 |
| Labeler Name: | Nature's Innovation, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20111001 |
Package Information of Naturasil
| Package NDC: | 10893-625-30 |
| Package Description: | 1 BOTTLE, GLASS in 1 CARTON (10893-625-30) > 1 LIQUID in 1 BOTTLE, GLASS |
NDC Information of Naturasil
| NDC Code | 10893-625-30 |
| Proprietary Name | Naturasil |
| Package Description | 1 BOTTLE, GLASS in 1 CARTON (10893-625-30) > 1 LIQUID in 1 BOTTLE, GLASS |
| Product NDC | 10893-625 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Sulfur |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20111001 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | Nature's Innovation, Inc. |
| Substance Name | SULFUR |
| Strength Number | 6 |
| Strength Unit | [hp_X]/1 |
| Pharmaceutical Classes |
