Skin Crave All Natural SPF30 is a Topical Lotion in the Human Otc Drug category. It is labeled and distributed by Tropical Enterprises International, Inc. The primary component is Titanium Dioxide; Zinc Oxide.
| Product ID | 58418-424_709870ff-e7c6-0fc8-e053-2a91aa0a737f |
| NDC | 58418-424 |
| Product Type | Human Otc Drug |
| Proprietary Name | Skin Crave All Natural SPF30 |
| Generic Name | All Natural Spf30 Sunscreen Lotion |
| Dosage Form | Lotion |
| Route of Administration | TOPICAL |
| Marketing Start Date | 2014-08-01 |
| Marketing Category | OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL |
| Application Number | part352 |
| Labeler Name | Tropical Enterprises International, Inc |
| Substance Name | TITANIUM DIOXIDE; ZINC OXIDE |
| Active Ingredient Strength | 10 mg/mL; mg/mL |
| NDC Exclude Flag | N |
| Listing Certified Through | 2019-12-31 |
| Marketing Start Date | 2014-08-01 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | OTC monograph not final |
| Application Number | part352 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2014-08-01 |
| Marketing End Date | 2020-01-01 |
| Inactivation Date | 2020-01-31 |
| Reactivation Date | 2020-04-28 |
| Marketing Category | OTC monograph not final |
| Application Number | part352 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2014-08-01 |
| Marketing End Date | 2020-01-01 |
| Inactivation Date | 2020-01-31 |
| Reactivation Date | 2020-04-28 |
| Marketing Category | OTC monograph not final |
| Application Number | part352 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2014-08-01 |
| Marketing End Date | 2020-01-01 |
| Inactivation Date | 2020-01-31 |
| Reactivation Date | 2020-04-28 |
| Marketing Category | OTC monograph not final |
| Application Number | part352 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2014-08-01 |
| Marketing End Date | 2020-01-01 |
| Inactivation Date | 2020-01-31 |
| Reactivation Date | 2020-04-28 |
| Marketing Category | OTC monograph not final |
| Application Number | part352 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2014-08-01 |
| Marketing End Date | 2020-01-01 |
| Inactivation Date | 2020-01-31 |
| Reactivation Date | 2020-04-28 |
| Marketing Category | OTC monograph not final |
| Application Number | part352 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2014-08-01 |
| Marketing End Date | 2020-01-01 |
| Inactivation Date | 2020-01-31 |
| Reactivation Date | 2020-04-28 |
| Marketing Category | OTC monograph not final |
| Application Number | part352 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2014-08-01 |
| Marketing End Date | 2020-01-01 |
| Inactivation Date | 2020-01-31 |
| Reactivation Date | 2020-04-28 |
| Ingredient | Strength |
|---|---|
| TITANIUM DIOXIDE | 10 mg/mL |
| SPL SET ID: | 6e142109-f9e4-34fd-e053-2a91aa0a0e9a |
| Manufacturer | |
| UNII |