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Parsol Suncare SPF 29
Parsol Suncare SPF 29 - 68572-6007-4 - (Oxybenzone, Octinoxate, Octisalate, Homosalate, and Avobenzone)
Drug Information of Parsol Suncare SPF 29
| Product NDC: | 68572-6007 |
| Proprietary Name: | Parsol Suncare SPF 29 |
| Non Proprietary Name: | Oxybenzone, Octinoxate, Octisalate, Homosalate, and Avobenzone |
| Active Ingredient(s): | 2.4; 5.9; 8.9; 5.9; 5.9 g/118mL; g/118mL; g/118mL; g/118mL; g/118mL & nbsp; Oxybenzone, Octinoxate, Octisalate, Homosalate, and Avobenzone |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Parsol Suncare SPF 29
| Product NDC: | 68572-6007 |
| Labeler Name: | Kara Vita, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20040101 |
Package Information of Parsol Suncare SPF 29
| Package NDC: | 68572-6007-4 |
| Package Description: | 1 BOTTLE in 1 CARTON (68572-6007-4) > 59 mL in 1 BOTTLE |
NDC Information of Parsol Suncare SPF 29
| NDC Code | 68572-6007-4 |
| Proprietary Name | Parsol Suncare SPF 29 |
| Package Description | 1 BOTTLE in 1 CARTON (68572-6007-4) > 59 mL in 1 BOTTLE |
| Product NDC | 68572-6007 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Oxybenzone, Octinoxate, Octisalate, Homosalate, and Avobenzone |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20040101 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Kara Vita, Inc. |
| Substance Name | AVOBENZONE; HOMOSALATE; OCTINOXATE; OCTISALATE; OXYBENZONE |
| Strength Number | 2.4; 5.9; 8.9; 5.9; 5.9 |
| Strength Unit | g/118mL; g/118mL; g/118mL; g/118mL; g/118mL |
| Pharmaceutical Classes |
