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 |