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POISON OAK
POISON OAK - 57479-101-13 - (HYDROCORTISONE, PHENOL)
Drug Information of POISON OAK
| Product NDC: | 57479-101 |
| Proprietary Name: | POISON OAK |
| Non Proprietary Name: | HYDROCORTISONE, PHENOL |
| Active Ingredient(s): | 1; .5 g/100g; g/100g & nbsp; HYDROCORTISONE, PHENOL |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of POISON OAK
| Product NDC: | 57479-101 |
| Labeler Name: | DeMartini Spring Hill Pharmacy, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20121129 |
Package Information of POISON OAK
| Package NDC: | 57479-101-13 |
| Package Description: | 100 g in 1 TUBE (57479-101-13) |
NDC Information of POISON OAK
| NDC Code | 57479-101-13 |
| Proprietary Name | POISON OAK |
| Package Description | 100 g in 1 TUBE (57479-101-13) |
| Product NDC | 57479-101 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | HYDROCORTISONE, PHENOL |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20121129 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | DeMartini Spring Hill Pharmacy, Inc. |
| Substance Name | HYDROCORTISONE; PHENOL |
| Strength Number | 1; .5 |
| Strength Unit | g/100g; g/100g |
| Pharmaceutical Classes |
