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DR. WALTONS
DR. WALTONS - 76271-001-02 - (TALC)
Drug Information of DR. WALTONS
| Product NDC: | 76271-001 |
| Proprietary Name: | DR. WALTONS |
| Non Proprietary Name: | TALC |
| Active Ingredient(s): | 5.2; 5.13 g/675g; g/675g & nbsp; TALC |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | POWDER |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of DR. WALTONS
| Product NDC: | 76271-001 |
| Labeler Name: | Dr. Waltons, Incorporated |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part347 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110709 |
Package Information of DR. WALTONS
| Package NDC: | 76271-001-02 |
| Package Description: | 55 g in 1 BOTTLE, PLASTIC (76271-001-02) |
NDC Information of DR. WALTONS
| NDC Code | 76271-001-02 |
| Proprietary Name | DR. WALTONS |
| Package Description | 55 g in 1 BOTTLE, PLASTIC (76271-001-02) |
| Product NDC | 76271-001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | TALC |
| Dosage Form Name | POWDER |
| Route Name | TOPICAL |
| Start Marketing Date | 20110709 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Dr. Waltons, Incorporated |
| Substance Name | ALPHA-TOCOPHEROL; ZINC OXIDE |
| Strength Number | 5.2; 5.13 |
| Strength Unit | g/675g; g/675g |
| Pharmaceutical Classes |
