Allegra Intensive Relief Anti-Itch is a Topical Cream in the Human Otc Drug category. It is labeled and distributed by Chattem, Inc.. The primary component is Allantoin; Diphenhydramine Hydrochloride.
| Product ID | 41167-4266_45a42766-0f7a-4c25-9dc2-50219b6cdf3a |
| NDC | 41167-4266 |
| Product Type | Human Otc Drug |
| Proprietary Name | Allegra Intensive Relief Anti-Itch |
| Generic Name | Diphenhydramine Hcl, Allantoin |
| Dosage Form | Cream |
| Route of Administration | TOPICAL |
| Marketing Start Date | 2012-12-01 |
| Marketing Category | OTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL |
| Application Number | part347 |
| Labeler Name | Chattem, Inc. |
| Substance Name | ALLANTOIN; DIPHENHYDRAMINE HYDROCHLORIDE |
| Active Ingredient Strength | 1 g/100g; g/100g |
| NDC Exclude Flag | N |
| Listing Certified Through | 2019-12-31 |
| Marketing Start Date | 2012-12-01 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | OTC MONOGRAPH FINAL |
| Application Number | part347 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2012-12-01 |
| Marketing End Date | 2018-04-15 |
| Marketing Category | OTC MONOGRAPH FINAL |
| Application Number | part347 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2012-12-01 |
| Marketing End Date | 2019-10-23 |
| Marketing Category | OTC MONOGRAPH FINAL |
| Application Number | part347 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2012-12-01 |
| Marketing End Date | 2019-04-21 |
| Ingredient | Strength |
|---|---|
| ALLANTOIN | .5 g/100g |
| SPL SET ID: | 5375b99c-ad91-409f-850d-9ea0003b32d3 |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 41167-4266 | Allegra Intensive Relief Anti-Itch | Diphenhydramine HCl, Allantoin |
| 41167-4255 | Allegra Cooling Relief Anti-Itch | Diphenhydramine HCl, Allantoin |