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SunScreen SPF30
SunScreen SPF30 - 31190-200-10 - (HOMOSALATE, OCTINOXATE, OCTISALATE, OXYBENZONE)
Drug Information of SunScreen SPF30
| Product NDC: | 31190-200 |
| Proprietary Name: | SunScreen SPF30 |
| Non Proprietary Name: | HOMOSALATE, OCTINOXATE, OCTISALATE, OXYBENZONE |
| Active Ingredient(s): | 5; 7.5; 5; 4.25 mL/100mL; mL/100mL; mL/100mL; mL/100mL & nbsp; HOMOSALATE, OCTINOXATE, OCTISALATE, OXYBENZONE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SunScreen SPF30
| Product NDC: | 31190-200 |
| Labeler Name: | Shanghai Kejing Cleaning Products Co., Ltd. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100415 |
Package Information of SunScreen SPF30
| Package NDC: | 31190-200-10 |
| Package Description: | 1 BOTTLE, SPRAY in 1 CARTON (31190-200-10) > 10 mL in 1 BOTTLE, SPRAY |
NDC Information of SunScreen SPF30
| NDC Code | 31190-200-10 |
| Proprietary Name | SunScreen SPF30 |
| Package Description | 1 BOTTLE, SPRAY in 1 CARTON (31190-200-10) > 10 mL in 1 BOTTLE, SPRAY |
| Product NDC | 31190-200 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | HOMOSALATE, OCTINOXATE, OCTISALATE, OXYBENZONE |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20100415 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Shanghai Kejing Cleaning Products Co., Ltd. |
| Substance Name | HOMOSALATE; OCTINOXATE; OCTISALATE; OXYBENZONE |
| Strength Number | 5; 7.5; 5; 4.25 |
| Strength Unit | mL/100mL; mL/100mL; mL/100mL; mL/100mL |
| Pharmaceutical Classes |
