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PETROLATUM
PETROLATUM - 67777-211-07 - (PETROLATUM)
Drug Information of PETROLATUM
| Product NDC: | 67777-211 |
| Proprietary Name: | PETROLATUM |
| Non Proprietary Name: | PETROLATUM |
| Active Ingredient(s): | 1 g/g & nbsp; PETROLATUM |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | JELLY |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of PETROLATUM
| Product NDC: | 67777-211 |
| Labeler Name: | Dynarex Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part347 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100131 |
Package Information of PETROLATUM
| Package NDC: | 67777-211-07 |
| Package Description: | 6 TUBE in 1 BOX (67777-211-07) > 113.4 g in 1 TUBE |
NDC Information of PETROLATUM
| NDC Code | 67777-211-07 |
| Proprietary Name | PETROLATUM |
| Package Description | 6 TUBE in 1 BOX (67777-211-07) > 113.4 g in 1 TUBE |
| Product NDC | 67777-211 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | PETROLATUM |
| Dosage Form Name | JELLY |
| Route Name | TOPICAL |
| Start Marketing Date | 20100131 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Dynarex Corporation |
| Substance Name | PETROLATUM |
| Strength Number | 1 |
| Strength Unit | g/g |
| Pharmaceutical Classes |
