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SunscreenSPF 30
SunscreenSPF 30 - 75857-2302-0 - (Octinoxate, Octisalate, Oxybenzone, Titanium Dioxide)
Drug Information of SunscreenSPF 30
| Product NDC: | 75857-2302 |
| Proprietary Name: | SunscreenSPF 30 |
| Non Proprietary Name: | Octinoxate, Octisalate, Oxybenzone, Titanium Dioxide |
| Active Ingredient(s): | 75; 20; 40; 2.5 mg/mL; mg/mL; mg/mL; mg/mL & nbsp; Octinoxate, Octisalate, Oxybenzone, Titanium Dioxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SunscreenSPF 30
| Product NDC: | 75857-2302 |
| Labeler Name: | Ningbo Dowland Daily Health Co., Ltd |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20130207 |
Package Information of SunscreenSPF 30
| Package NDC: | 75857-2302-0 |
| Package Description: | 20 mL in 1 BOTTLE (75857-2302-0) |
NDC Information of SunscreenSPF 30
| NDC Code | 75857-2302-0 |
| Proprietary Name | SunscreenSPF 30 |
| Package Description | 20 mL in 1 BOTTLE (75857-2302-0) |
| Product NDC | 75857-2302 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Octinoxate, Octisalate, Oxybenzone, Titanium Dioxide |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20130207 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Ningbo Dowland Daily Health Co., Ltd |
| Substance Name | OCTINOXATE; OCTISALATE; OXYBENZONE; TITANIUM DIOXIDE |
| Strength Number | 75; 20; 40; 2.5 |
| Strength Unit | mg/mL; mg/mL; mg/mL; mg/mL |
| Pharmaceutical Classes |
