NDC 51414-201
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 Commodity Co.,ltd.. The primary component is Octinoxate; Oxybenzone; Titanium Dioxide; Homosalate.
| Product ID | 51414-201_6259609f-862a-1472-e053-2991aa0a10a2 |
| NDC | 51414-201 |
| 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 Commodity Co.,Ltd. |
| Substance Name | OCTINOXATE; OXYBENZONE; TITANIUM DIOXIDE; HOMOSALATE |
| Active Ingredient Strength | 8 g/100g; g/100g; g/100g; g/100g |
| NDC Exclude Flag | N |
| Listing Certified Through | 2020-12-31 |
Packaging
NDC 51414-201-01
15 g in 1 BOTTLE (51414-201-01)
| Marketing Start Date | 2018-01-10 |
| NDC Exclude Flag | N |
| Sample Package? | N |
NDC SPL Data Element Entries
NDC 51414-201-15 [51414020115]
Sun Block CREAM
| Marketing Category | OTC monograph final |
| Application Number | part352 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2018-01-10 |
NDC 51414-201-06 [51414020106]
Sun Block CREAM
| Marketing Category | OTC monograph final |
| Application Number | part352 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2018-01-10 |
NDC 51414-201-13 [51414020113]
Sun Block CREAM
| Marketing Category | OTC monograph final |
| Application Number | part352 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2018-01-10 |
NDC 51414-201-01 [51414020101]
Sun Block CREAM
| Marketing Category | OTC monograph final |
| Application Number | part352 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2018-01-10 |
NDC 51414-201-02 [51414020102]
Sun Block CREAM
| Marketing Category | OTC monograph final |
| Application Number | part352 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2018-01-10 |
NDC 51414-201-04 [51414020104]
Sun Block CREAM
| Marketing Category | OTC monograph final |
| Application Number | part352 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2018-01-10 |
NDC 51414-201-05 [51414020105]
Sun Block CREAM
| Marketing Category | OTC monograph final |
| Application Number | part352 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2018-01-10 |
NDC 51414-201-08 [51414020108]
Sun Block CREAM
| Marketing Category | OTC monograph final |
| Application Number | part352 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2018-01-10 |
NDC 51414-201-12 [51414020112]
Sun Block CREAM
| Marketing Category | OTC monograph final |
| Application Number | part352 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2018-01-10 |
NDC 51414-201-11 [51414020111]
Sun Block CREAM
| Marketing Category | OTC monograph final |
| Application Number | part352 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2018-01-10 |
NDC 51414-201-10 [51414020110]
Sun Block CREAM
| Marketing Category | OTC monograph final |
| Application Number | part352 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2018-01-10 |
NDC 51414-201-09 [51414020109]
Sun Block CREAM
| Marketing Category | OTC monograph final |
| Application Number | part352 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2018-01-10 |
NDC 51414-201-03 [51414020103]
Sun Block CREAM
| Marketing Category | OTC monograph final |
| Application Number | part352 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2018-01-10 |
NDC 51414-201-07 [51414020107]
Sun Block CREAM
| Marketing Category | OTC monograph final |
| Application Number | part352 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2018-01-10 |
NDC 51414-201-14 [51414020114]
Sun Block CREAM
| Marketing Category | OTC monograph final |
| Application Number | part352 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2018-01-10 |
Drug Details
Active Ingredients
| Ingredient | Strength |
|---|---|
| OCTINOXATE | 8 g/100g |
OpenFDA Data
| SPL SET ID: | 6259609f-8629-1472-e053-2991aa0a10a2 |
| 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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