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SPF 30 Sunscreen
SPF 30 Sunscreen - 57817-300-07 - (OCTINOXATE OXYBENZONE Octisalate)
Drug Information of SPF 30 Sunscreen
| Product NDC: | 57817-300 |
| Proprietary Name: | SPF 30 Sunscreen |
| Non Proprietary Name: | OCTINOXATE OXYBENZONE Octisalate |
| Active Ingredient(s): | 6; 5; 4 g/100g; g/100g; g/100g & nbsp; OCTINOXATE OXYBENZONE Octisalate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SPRAY |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SPF 30 Sunscreen
| Product NDC: | 57817-300 |
| Labeler Name: | Hangzhou Haorun Technology CO.,LTD. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20130418 |
Package Information of SPF 30 Sunscreen
| Package NDC: | 57817-300-07 |
| Package Description: | 35 g in 1 BOTTLE (57817-300-07) |
NDC Information of SPF 30 Sunscreen
| NDC Code | 57817-300-07 |
| Proprietary Name | SPF 30 Sunscreen |
| Package Description | 35 g in 1 BOTTLE (57817-300-07) |
| Product NDC | 57817-300 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE OXYBENZONE Octisalate |
| Dosage Form Name | SPRAY |
| Route Name | TOPICAL |
| Start Marketing Date | 20130418 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Hangzhou Haorun Technology CO.,LTD. |
| Substance Name | OCTINOXATE; OCTISALATE; OXYBENZONE |
| Strength Number | 6; 5; 4 |
| Strength Unit | g/100g; g/100g; g/100g |
| Pharmaceutical Classes |
