| Product NDC: | 59779-717 |
| Proprietary Name: | CAMPHOR, EUCALYPTUS OIL and MENTHOL |
| Non Proprietary Name: | CAMPHOR, EUCALYPTUS OIL and MENTHOL |
| Active Ingredient(s): | 52; 12; 28 mg/mL; mg/mL; mg/mL & nbsp; CAMPHOR, EUCALYPTUS OIL and MENTHOL |
| Administration Route(s): | RESPIRATORY (INHALATION) |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 59779-717 |
| Labeler Name: | CVS |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20090519 |
| Package NDC: | 59779-717-01 |
| Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (59779-717-01) > 237 mL in 1 BOTTLE, PLASTIC |
| NDC Code | 59779-717-01 |
| Proprietary Name | CAMPHOR, EUCALYPTUS OIL and MENTHOL |
| Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (59779-717-01) > 237 mL in 1 BOTTLE, PLASTIC |
| Product NDC | 59779-717 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | CAMPHOR, EUCALYPTUS OIL and MENTHOL |
| Dosage Form Name | OINTMENT |
| Route Name | RESPIRATORY (INHALATION) |
| Start Marketing Date | 20090519 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | CVS |
| Substance Name | CAMPHOR (SYNTHETIC); EUCALYPTUS OIL; MENTHOL |
| Strength Number | 52; 12; 28 |
| Strength Unit | mg/mL; mg/mL; mg/mL |
| Pharmaceutical Classes |