Skin Crave spf30 sunscreen is a Topical Lotion in the Human Otc Drug category. It is labeled and distributed by Tropical Enterprises International, Inc.. The primary component is Octisalate; Oxybenzone; Octocrylene; Octinoxate.
| Product ID | 58418-223_092bafd9-8c28-56df-e054-00144ff88e88 |
| NDC | 58418-223 |
| Product Type | Human Otc Drug |
| Proprietary Name | Skin Crave spf30 sunscreen |
| Generic Name | Spf30 Sunscreen Lotion (non-broad Spectrum) |
| Dosage Form | Lotion |
| Route of Administration | TOPICAL |
| Marketing Start Date | 2012-08-01 |
| Marketing Category | OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL |
| Application Number | part352 |
| Labeler Name | Tropical Enterprises International, Inc. |
| Substance Name | OCTISALATE; OXYBENZONE; OCTOCRYLENE; OCTINOXATE |
| Active Ingredient Strength | 4 mg/mL; mg/mL; mg/mL; mg/mL |
| NDC Exclude Flag | E |
| Listing Certified Through | 2018-12-31 |
| Marketing Start Date | 2012-08-01 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | OTC monograph not final |
| Application Number | part352 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2012-08-01 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | OTC monograph not final |
| Application Number | part352 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2012-08-01 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | OTC monograph not final |
| Application Number | part352 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2012-08-01 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | OTC monograph not final |
| Application Number | part352 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2012-08-01 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | OTC monograph not final |
| Application Number | part352 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2012-08-01 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | OTC monograph not final |
| Application Number | part352 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2012-08-01 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | OTC monograph not final |
| Application Number | part352 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2012-08-01 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | OTC monograph not final |
| Application Number | part352 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2012-08-01 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | OTC monograph not final |
| Application Number | part352 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2012-08-01 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | OTC monograph not final |
| Application Number | part352 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2012-08-01 |
| Inactivation Date | 2020-01-31 |
| Ingredient | Strength |
|---|---|
| OCTISALATE | 4 mg/mL |
| SPL SET ID: | 092bafd9-8c27-56df-e054-00144ff88e88 |
| Manufacturer | |
| UNII |