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Allegra Intensive Relief Anti-Itch
Allegra Intensive Relief Anti-Itch - 41167-4266-0 - (Diphenhydramine HCl, Allantoin)
Drug Information of Allegra Intensive Relief Anti-Itch
| Product NDC: | 41167-4266 |
| Proprietary Name: | Allegra Intensive Relief Anti-Itch |
| Non Proprietary Name: | Diphenhydramine HCl, Allantoin |
| Active Ingredient(s): | .5; 2 g/100g; g/100g & nbsp; Diphenhydramine HCl, Allantoin |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Allegra Intensive Relief Anti-Itch
| Product NDC: | 41167-4266 |
| Labeler Name: | Chattem, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part347 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20121201 |
Package Information of Allegra Intensive Relief Anti-Itch
| Package NDC: | 41167-4266-0 |
| Package Description: | 1 TUBE in 1 CARTON (41167-4266-0) > 28.3 g in 1 TUBE |
NDC Information of Allegra Intensive Relief Anti-Itch
| NDC Code | 41167-4266-0 |
| Proprietary Name | Allegra Intensive Relief Anti-Itch |
| Package Description | 1 TUBE in 1 CARTON (41167-4266-0) > 28.3 g in 1 TUBE |
| Product NDC | 41167-4266 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Diphenhydramine HCl, Allantoin |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20121201 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Chattem, Inc. |
| Substance Name | ALLANTOIN; DIPHENHYDRAMINE HYDROCHLORIDE |
| Strength Number | .5; 2 |
| Strength Unit | g/100g; g/100g |
| Pharmaceutical Classes |
