Product NDC: | 10742-0001 |
Proprietary Name: | Mentholatum |
Non Proprietary Name: | Camphor, menthol |
Active Ingredient(s): | 90; 13 mg/g; mg/g & nbsp; Camphor, menthol |
Administration Route(s): | TOPICAL |
Dosage Form(s): | OINTMENT |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 10742-0001 |
Labeler Name: | The Mentholatum Company |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part348 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 19761213 |
Package NDC: | 10742-0001-2 |
Package Description: | 1 JAR in 1 CARTON (10742-0001-2) > 85 g in 1 JAR |
NDC Code | 10742-0001-2 |
Proprietary Name | Mentholatum |
Package Description | 1 JAR in 1 CARTON (10742-0001-2) > 85 g in 1 JAR |
Product NDC | 10742-0001 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Camphor, menthol |
Dosage Form Name | OINTMENT |
Route Name | TOPICAL |
Start Marketing Date | 19761213 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | The Mentholatum Company |
Substance Name | CAMPHOR (SYNTHETIC); MENTHOL |
Strength Number | 90; 13 |
Strength Unit | mg/g; mg/g |
Pharmaceutical Classes |