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Face and Body Sunscreen SPF 35
Face and Body Sunscreen SPF 35 - 68828-166-02 - (Avobenzone, Homosalate, Octisalate, Octocrylene, Oxybenzone)
Drug Information of Face and Body Sunscreen SPF 35
| Product NDC: | 68828-166 |
| Proprietary Name: | Face and Body Sunscreen SPF 35 |
| Non Proprietary Name: | Avobenzone, Homosalate, Octisalate, Octocrylene, Oxybenzone |
| Active Ingredient(s): | 3; 10; 5; 2.79; 6 g/100mL; g/100mL; g/100mL; g/100mL; g/100mL & nbsp; Avobenzone, Homosalate, Octisalate, Octocrylene, Oxybenzone |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SPRAY |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Face and Body Sunscreen SPF 35
| Product NDC: | 68828-166 |
| Labeler Name: | JAFRA COSMETICS INTERNATIONAL |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20130110 |
Package Information of Face and Body Sunscreen SPF 35
| Package NDC: | 68828-166-02 |
| Package Description: | 1 BOTTLE in 1 CARTON (68828-166-02) > 125 mL in 1 BOTTLE (68828-166-01) |
NDC Information of Face and Body Sunscreen SPF 35
| NDC Code | 68828-166-02 |
| Proprietary Name | Face and Body Sunscreen SPF 35 |
| Package Description | 1 BOTTLE in 1 CARTON (68828-166-02) > 125 mL in 1 BOTTLE (68828-166-01) |
| Product NDC | 68828-166 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Avobenzone, Homosalate, Octisalate, Octocrylene, Oxybenzone |
| Dosage Form Name | SPRAY |
| Route Name | TOPICAL |
| Start Marketing Date | 20130110 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | JAFRA COSMETICS INTERNATIONAL |
| Substance Name | AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE |
| Strength Number | 3; 10; 5; 2.79; 6 |
| Strength Unit | g/100mL; g/100mL; g/100mL; g/100mL; g/100mL |
| Pharmaceutical Classes |
