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Hydrocortisone anti-itch plus
Hydrocortisone anti-itch plus - 49035-732-20 - (Hydrocortisone)
Drug Information of Hydrocortisone anti-itch plus
| Product NDC: | 49035-732 |
| Proprietary Name: | Hydrocortisone anti-itch plus |
| Non Proprietary Name: | Hydrocortisone |
| Active Ingredient(s): | 10 mg/g & nbsp; Hydrocortisone |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Hydrocortisone anti-itch plus
| Product NDC: | 49035-732 |
| Labeler Name: | Wal-Mart Stores, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100601 |
Package Information of Hydrocortisone anti-itch plus
| Package NDC: | 49035-732-20 |
| Package Description: | 1 TUBE in 1 CARTON (49035-732-20) > 60 g in 1 TUBE |
NDC Information of Hydrocortisone anti-itch plus
| NDC Code | 49035-732-20 |
| Proprietary Name | Hydrocortisone anti-itch plus |
| Package Description | 1 TUBE in 1 CARTON (49035-732-20) > 60 g in 1 TUBE |
| Product NDC | 49035-732 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Hydrocortisone |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20100601 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Wal-Mart Stores, Inc. |
| Substance Name | HYDROCORTISONE |
| Strength Number | 10 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
