Mentholatum Natural Ice Original is a Topical Ointment in the Human Otc Drug category. It is labeled and distributed by The Mentholatum Company. The primary component is Dimethicone; Octinoxate; Octisalate.
| Product ID | 10742-3004_24cc4906-53dd-495d-8d02-f6ea8b6b584f |
| NDC | 10742-3004 |
| Product Type | Human Otc Drug |
| Proprietary Name | Mentholatum Natural Ice Original |
| Generic Name | Dimethicone, Octinoxate, Octisalate |
| Dosage Form | Ointment |
| Route of Administration | TOPICAL |
| Marketing Start Date | 1999-01-19 |
| Marketing Category | OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL |
| Application Number | part352 |
| Labeler Name | The Mentholatum Company |
| Substance Name | DIMETHICONE; OCTINOXATE; OCTISALATE |
| Active Ingredient Strength | 10 mg/g; mg/g; mg/g |
| NDC Exclude Flag | N |
| Listing Certified Through | 2022-12-31 |
| Marketing Start Date | 2019-04-02 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | OTC monograph not final |
| Application Number | part352 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2019-04-02 |
| Marketing Category | OTC monograph not final |
| Application Number | part352 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 1999-01-19 |
| Marketing End Date | 2014-10-08 |
| Marketing Category | OTC monograph not final |
| Application Number | part352 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 1999-01-19 |
| Marketing End Date | 2019-04-01 |
| Marketing Category | OTC monograph not final |
| Application Number | part352 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 1999-01-19 |
| Marketing Category | OTC monograph not final |
| Application Number | part352 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 1999-01-19 |
| Marketing Category | OTC monograph not final |
| Application Number | part352 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 1999-01-19 |
| Marketing End Date | 2019-04-01 |
| Marketing Category | OTC monograph not final |
| Application Number | part352 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2019-04-02 |
| Ingredient | Strength |
|---|---|
| DIMETHICONE | 10 mg/g |
| SPL SET ID: | 29220eaa-87cb-4ebe-87db-d36288b3a9e4 |
| Manufacturer | |
| UNII |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 10742-8865 | Mentholatum Medicated Lip Balm | dimethicone, octinoxate, octisalate |
| 10742-8893 | Mentholatum Medicated Lip Balm | dimethicone, octinoxate, octisalate |
| 10742-1048 | Mentholatum Natural Ice | dimethicone, octinoxate, octisalate |
| 10742-3004 | Mentholatum Natural Ice | dimethicone, octinoxate, octisalate |