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Lanolin
Lanolin - 67777-232-04 - (Lanolin)
Drug Information of Lanolin
| Product NDC: | 67777-232 |
| Proprietary Name: | Lanolin |
| Non Proprietary Name: | Lanolin |
| Active Ingredient(s): | 50 g/100g & nbsp; Lanolin |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Lanolin
| Product NDC: | 67777-232 |
| Labeler Name: | Dynarex Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part347 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100512 |
Package Information of Lanolin
| Package NDC: | 67777-232-04 |
| Package Description: | 24 TUBE in 1 CASE (67777-232-04) > 113 g in 1 TUBE |
NDC Information of Lanolin
| NDC Code | 67777-232-04 |
| Proprietary Name | Lanolin |
| Package Description | 24 TUBE in 1 CASE (67777-232-04) > 113 g in 1 TUBE |
| Product NDC | 67777-232 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Lanolin |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 20100512 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Dynarex Corporation |
| Substance Name | LANOLIN |
| Strength Number | 50 |
| Strength Unit | g/100g |
| Pharmaceutical Classes |
