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Sun Protection Face SPF 30
Sun Protection Face SPF 30 - 68026-422-07 - (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE)
Drug Information of Sun Protection Face SPF 30
| Product NDC: | 68026-422 |
| Proprietary Name: | Sun Protection Face SPF 30 |
| Non Proprietary Name: | AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE |
| Active Ingredient(s): | 3; 10; 2.6; 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): | EMULSION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sun Protection Face SPF 30
| Product NDC: | 68026-422 |
| Labeler Name: | La Prairie, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110408 |
Package Information of Sun Protection Face SPF 30
| Package NDC: | 68026-422-07 |
| Package Description: | 7 mL in 1 BOTTLE (68026-422-07) |
NDC Information of Sun Protection Face SPF 30
| NDC Code | 68026-422-07 |
| Proprietary Name | Sun Protection Face SPF 30 |
| Package Description | 7 mL in 1 BOTTLE (68026-422-07) |
| Product NDC | 68026-422 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE |
| Dosage Form Name | EMULSION |
| Route Name | TOPICAL |
| Start Marketing Date | 20110408 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | La Prairie, Inc. |
| Substance Name | AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE |
| Strength Number | 3; 10; 2.6; 2.4; 5 |
| Strength Unit | mL/100mL; mL/100mL; mL/100mL; mL/100mL; mL/100mL |
| Pharmaceutical Classes |
