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Allure Creamy Petroleum
Allure Creamy Petroleum - 52000-000-00 - (PETROLATUM)
Drug Information of Allure Creamy Petroleum
| Product NDC: | 52000-000 |
| Proprietary Name: | Allure Creamy Petroleum |
| Non Proprietary Name: | PETROLATUM |
| Active Ingredient(s): | 30 g/100g & nbsp; PETROLATUM |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | JELLY |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Allure Creamy Petroleum
| Product NDC: | 52000-000 |
| Labeler Name: | Universal Distribution Center LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part347 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20121219 |
Package Information of Allure Creamy Petroleum
| Package NDC: | 52000-000-00 |
| Package Description: | 200 g in 1 TUBE (52000-000-00) |
NDC Information of Allure Creamy Petroleum
| NDC Code | 52000-000-00 |
| Proprietary Name | Allure Creamy Petroleum |
| Package Description | 200 g in 1 TUBE (52000-000-00) |
| Product NDC | 52000-000 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | PETROLATUM |
| Dosage Form Name | JELLY |
| Route Name | TOPICAL |
| Start Marketing Date | 20121219 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Universal Distribution Center LLC |
| Substance Name | PETROLATUM |
| Strength Number | 30 |
| Strength Unit | g/100g |
| Pharmaceutical Classes |
