NDC 51414-200
Sun Block
Octyl Methoxycinnamate Benzophenone-3 Titanium Dioxide Homosalate
Sun Block is a Topical Cream in the Human Otc Drug category. It is labeled and distributed by Yuyao Jessie Promotional Products Co., Ltd.. The primary component is Octinoxate; Oxybenzone; Titanium Dioxide; Homosalate.
| Product ID | 51414-200_ead90432-b6f9-457d-a022-b0c76a2e9d24 |
| NDC | 51414-200 |
| Product Type | Human Otc Drug |
| Proprietary Name | Sun Block |
| Generic Name | Octyl Methoxycinnamate Benzophenone-3 Titanium Dioxide Homosalate |
| Dosage Form | Cream |
| Route of Administration | TOPICAL |
| Marketing Start Date | 2010-06-30 |
| Marketing Category | OTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL |
| Application Number | part352 |
| Labeler Name | Yuyao Jessie Promotional Products Co., Ltd. |
| Substance Name | OCTINOXATE; OXYBENZONE; TITANIUM DIOXIDE; HOMOSALATE |
| Active Ingredient Strength | 8 mL/100mL; mL/100mL; mL/100mL; mL/100mL |
| NDC Exclude Flag | E |
| Listing Certified Through | 2017-12-31 |
Packaging
NDC 51414-200-01
15 mL in 1 BOTTLE (51414-200-01)
| Marketing Start Date | 2010-06-30 |
| NDC Exclude Flag | N |
| Sample Package? | N |
NDC SPL Data Element Entries
NDC 51414-200-12 [51414020012]
Sun Block CREAM
| Marketing Category | OTC monograph final |
| Application Number | part352 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2010-06-30 |
| Inactivation Date | 2019-10-21 |
NDC 51414-200-04 [51414020004]
Sun Block CREAM
| Marketing Category | OTC monograph final |
| Application Number | part352 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2010-06-30 |
| Inactivation Date | 2019-10-21 |
NDC 51414-200-02 [51414020002]
Sun Block CREAM
| Marketing Category | OTC monograph final |
| Application Number | part352 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2010-06-30 |
| Inactivation Date | 2019-10-21 |
NDC 51414-200-14 [51414020014]
Sun Block CREAM
| Marketing Category | OTC monograph final |
| Application Number | part352 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2010-06-30 |
| Inactivation Date | 2019-10-21 |
NDC 51414-200-07 [51414020007]
Sun Block CREAM
| Marketing Category | OTC monograph final |
| Application Number | part352 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2010-06-30 |
| Inactivation Date | 2019-10-21 |
NDC 51414-200-13 [51414020013]
Sun Block CREAM
| Marketing Category | OTC monograph final |
| Application Number | part352 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2010-06-30 |
| Inactivation Date | 2019-10-21 |
NDC 51414-200-15 [51414020015]
Sun Block CREAM
| Marketing Category | OTC monograph final |
| Application Number | part352 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2010-06-30 |
| Inactivation Date | 2019-10-21 |
NDC 51414-200-06 [51414020006]
Sun Block CREAM
| Marketing Category | OTC monograph final |
| Application Number | part352 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2010-06-30 |
| Inactivation Date | 2019-10-21 |
NDC 51414-200-05 [51414020005]
Sun Block CREAM
| Marketing Category | OTC monograph final |
| Application Number | part352 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2010-06-30 |
| Inactivation Date | 2019-10-21 |
NDC 51414-200-03 [51414020003]
Sun Block CREAM
| Marketing Category | OTC monograph final |
| Application Number | part352 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2010-06-30 |
| Inactivation Date | 2019-10-21 |
NDC 51414-200-08 [51414020008]
Sun Block CREAM
| Marketing Category | OTC monograph final |
| Application Number | part352 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2010-06-30 |
| Inactivation Date | 2019-10-21 |
NDC 51414-200-09 [51414020009]
Sun Block CREAM
| Marketing Category | OTC monograph final |
| Application Number | part352 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2010-06-30 |
| Inactivation Date | 2019-10-21 |
NDC 51414-200-01 [51414020001]
Sun Block CREAM
| Marketing Category | OTC monograph final |
| Application Number | part352 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2010-06-30 |
| Inactivation Date | 2019-10-21 |
NDC 51414-200-11 [51414020011]
Sun Block CREAM
| Marketing Category | OTC monograph final |
| Application Number | part352 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2010-06-30 |
| Inactivation Date | 2019-10-21 |
NDC 51414-200-10 [51414020010]
Sun Block CREAM
| Marketing Category | OTC monograph final |
| Application Number | part352 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2010-06-30 |
| Inactivation Date | 2019-10-21 |
Drug Details
Active Ingredients
| Ingredient | Strength |
|---|---|
| OCTINOXATE | 8 mL/100mL |
OpenFDA Data
| SPL SET ID: | f9e0f06c-3c58-4070-b29b-7df35cc2aa4e |
| Manufacturer | |
| UNII |
NDC Crossover Matching brand name "Sun Block" or generic name "Octyl Methoxycinnamate Benzophenone-3 Titanium Dioxide Homosalate"
| NDC | Brand Name | Generic Name |
|---|---|---|
| 51414-200 | Sun Block | octyl methoxycinnamate BENZOPHENONE-3 TITANIUM DIOXIDE Homosalate |
| 51414-201 | Sun Block | octyl methoxycinnamate BENZOPHENONE-3 TITANIUM DIOXIDE Homosalate |
Trademark Results [Sun Block]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 SUN BLOCK 76591559 not registered Dead/Abandoned |
Fisher, Myles A. 2004-05-10 |
 SUN BLOCK 73375110 1361189 Dead/Cancelled |
TURTLE WAX, INC. 1982-07-19 |
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