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Sun Protection Emulsion Face
Sun Protection Emulsion Face - 59614-221-11 - (Avobenzone, Homosalate, octisalate, octocrylene, oxybenzone)
Drug Information of Sun Protection Emulsion Face
| Product NDC: | 59614-221 |
| Proprietary Name: | Sun Protection Emulsion Face |
| Non Proprietary Name: | Avobenzone, Homosalate, octisalate, octocrylene, oxybenzone |
| Active Ingredient(s): | 3; 10; 2.5; 2.4; 5 mL/100mL; mL/100mL; mL/100mL; mL/100mL; mL/100mL & nbsp; Avobenzone, Homosalate, octisalate, octocrylene, oxybenzone |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sun Protection Emulsion Face
| Product NDC: | 59614-221 |
| Labeler Name: | Juvena GMBH |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110214 |
Package Information of Sun Protection Emulsion Face
| Package NDC: | 59614-221-11 |
| Package Description: | .088 mL in 1 DRUM (59614-221-11) |
NDC Information of Sun Protection Emulsion Face
| NDC Code | 59614-221-11 |
| Proprietary Name | Sun Protection Emulsion Face |
| Package Description | .088 mL in 1 DRUM (59614-221-11) |
| Product NDC | 59614-221 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Avobenzone, Homosalate, octisalate, octocrylene, oxybenzone |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20110214 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Juvena GMBH |
| Substance Name | AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE |
| Strength Number | 3; 10; 2.5; 2.4; 5 |
| Strength Unit | mL/100mL; mL/100mL; mL/100mL; mL/100mL; mL/100mL |
| Pharmaceutical Classes |
