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Face and Body Sunscreen Spray
Face and Body Sunscreen Spray - 68828-092-01 - (Homosalate, Oxybenzone, Octinoxate, Octisalate, Octocrylene)
Drug Information of Face and Body Sunscreen Spray
| Product NDC: | 68828-092 |
| Proprietary Name: | Face and Body Sunscreen Spray |
| Non Proprietary Name: | Homosalate, Oxybenzone, Octinoxate, Octisalate, Octocrylene |
| Active Ingredient(s): | 10; 3; 5; 2.79; 6 mL/100mL; mL/100mL; mL/100mL; mL/100mL; mL/100mL & nbsp; Homosalate, Oxybenzone, Octinoxate, Octisalate, Octocrylene |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Face and Body Sunscreen Spray
| Product NDC: | 68828-092 |
| Labeler Name: | Jafra Cosmetics International Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20120605 |
Package Information of Face and Body Sunscreen Spray
| Package NDC: | 68828-092-01 |
| Package Description: | 1 BOTTLE in 1 BOX (68828-092-01) > 125 mL in 1 BOTTLE |
NDC Information of Face and Body Sunscreen Spray
| NDC Code | 68828-092-01 |
| Proprietary Name | Face and Body Sunscreen Spray |
| Package Description | 1 BOTTLE in 1 BOX (68828-092-01) > 125 mL in 1 BOTTLE |
| Product NDC | 68828-092 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Homosalate, Oxybenzone, Octinoxate, Octisalate, Octocrylene |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20120605 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Jafra Cosmetics International Inc |
| Substance Name | HOMOSALATE; OCTINOXATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE |
| Strength Number | 10; 3; 5; 2.79; 6 |
| Strength Unit | mL/100mL; mL/100mL; mL/100mL; mL/100mL; mL/100mL |
| Pharmaceutical Classes |
