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SPF 15 Sunscreen
SPF 15 Sunscreen - 75857-2153-0 - (OCTINOXATE, OXYBENZONE, OCTISALATE, TITANIUM DIOXIDE)
Drug Information of SPF 15 Sunscreen
| Product NDC: | 75857-2153 |
| Proprietary Name: | SPF 15 Sunscreen |
| Non Proprietary Name: | OCTINOXATE, OXYBENZONE, OCTISALATE, TITANIUM DIOXIDE |
| Active Ingredient(s): | 50; 10; 15; 20 mg/mL; mg/mL; mg/mL; mg/mL & nbsp; OCTINOXATE, OXYBENZONE, OCTISALATE, TITANIUM DIOXIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SPF 15 Sunscreen
| Product NDC: | 75857-2153 |
| 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: | 20130620 |
Package Information of SPF 15 Sunscreen
| Package NDC: | 75857-2153-0 |
| Package Description: | 1 BOTTLE in 1 CARTON (75857-2153-0) > 30 mL in 1 BOTTLE |
NDC Information of SPF 15 Sunscreen
| NDC Code | 75857-2153-0 |
| Proprietary Name | SPF 15 Sunscreen |
| Package Description | 1 BOTTLE in 1 CARTON (75857-2153-0) > 30 mL in 1 BOTTLE |
| Product NDC | 75857-2153 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE, OXYBENZONE, OCTISALATE, TITANIUM DIOXIDE |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20130620 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Ningbo Dowland Daily Health Co., Ltd |
| Substance Name | OCTINOXATE; OCTISALATE; OXYBENZONE; TITANIUM DIOXIDE |
| Strength Number | 50; 10; 15; 20 |
| Strength Unit | mg/mL; mg/mL; mg/mL; mg/mL |
| Pharmaceutical Classes |
