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SPF 50
SPF 50 - 49527-717-01 - (oxybenzone, octisalate, homosalate, avobenzone, and octocrylene)
Drug Information of SPF 50
| Product NDC: | 49527-717 |
| Proprietary Name: | SPF 50 |
| Non Proprietary Name: | oxybenzone, octisalate, homosalate, avobenzone, and octocrylene |
| Active Ingredient(s): | 3; 5; 5; 2.7; 5 mL/100mL; mL/100mL; mL/100mL; mL/100mL; mL/100mL & nbsp; oxybenzone, octisalate, homosalate, avobenzone, and octocrylene |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SPF 50
| Product NDC: | 49527-717 |
| Labeler Name: | CLINIQUE LABORATORIES INC. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20090101 |
Package Information of SPF 50
| Package NDC: | 49527-717-01 |
| Package Description: | 1 BOTTLE in 1 CARTON (49527-717-01) > 50 mL in 1 BOTTLE |
NDC Information of SPF 50
| NDC Code | 49527-717-01 |
| Proprietary Name | SPF 50 |
| Package Description | 1 BOTTLE in 1 CARTON (49527-717-01) > 50 mL in 1 BOTTLE |
| Product NDC | 49527-717 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | oxybenzone, octisalate, homosalate, avobenzone, and octocrylene |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20090101 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | CLINIQUE LABORATORIES INC. |
| Substance Name | AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE |
| Strength Number | 3; 5; 5; 2.7; 5 |
| Strength Unit | mL/100mL; mL/100mL; mL/100mL; mL/100mL; mL/100mL |
| Pharmaceutical Classes |
