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Sun Block
Sun Block - 51414-200-07 - (octyl methoxycinnamate BENZOPHENONE-3 TITANIUM DIOXIDE Homosalate)
Drug Information of Sun Block
| Product NDC: | 51414-200 |
| Proprietary Name: | Sun Block |
| Non Proprietary Name: | octyl methoxycinnamate BENZOPHENONE-3 TITANIUM DIOXIDE Homosalate |
| Active Ingredient(s): | 6; 8; 7.5; 8 mL/100mL; mL/100mL; mL/100mL; mL/100mL & nbsp; octyl methoxycinnamate BENZOPHENONE-3 TITANIUM DIOXIDE Homosalate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sun Block
| Product NDC: | 51414-200 |
| Labeler Name: | Yuyao Jessie Promotional Products Co., Ltd. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100630 |
Package Information of Sun Block
| Package NDC: | 51414-200-07 |
| Package Description: | 70 mL in 1 BOTTLE (51414-200-07) |
NDC Information of Sun Block
| NDC Code | 51414-200-07 |
| Proprietary Name | Sun Block |
| Package Description | 70 mL in 1 BOTTLE (51414-200-07) |
| Product NDC | 51414-200 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | octyl methoxycinnamate BENZOPHENONE-3 TITANIUM DIOXIDE Homosalate |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20100630 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Yuyao Jessie Promotional Products Co., Ltd. |
| Substance Name | HOMOSALATE; OCTINOXATE; OXYBENZONE; TITANIUM DIOXIDE |
| Strength Number | 6; 8; 7.5; 8 |
| Strength Unit | mL/100mL; mL/100mL; mL/100mL; mL/100mL |
| Pharmaceutical Classes |
