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Ultra Protection SPF 40
Ultra Protection SPF 40 - 68026-421-10 - (AVOBENZONE, HOMOSALATE, OCTISALATE, OXYBENZONE)
Drug Information of Ultra Protection SPF 40
| Product NDC: | 68026-421 |
| Proprietary Name: | Ultra Protection SPF 40 |
| Non Proprietary Name: | AVOBENZONE, HOMOSALATE, OCTISALATE, OXYBENZONE |
| Active Ingredient(s): | 3; 7; 5; 2 g/100g; g/100g; g/100g; g/100g & nbsp; AVOBENZONE, HOMOSALATE, OCTISALATE, OXYBENZONE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | STICK |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ultra Protection SPF 40
| Product NDC: | 68026-421 |
| Labeler Name: | La Prairie, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110407 |
Package Information of Ultra Protection SPF 40
| Package NDC: | 68026-421-10 |
| Package Description: | 10 g in 1 PACKAGE (68026-421-10) |
NDC Information of Ultra Protection SPF 40
| NDC Code | 68026-421-10 |
| Proprietary Name | Ultra Protection SPF 40 |
| Package Description | 10 g in 1 PACKAGE (68026-421-10) |
| Product NDC | 68026-421 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | AVOBENZONE, HOMOSALATE, OCTISALATE, OXYBENZONE |
| Dosage Form Name | STICK |
| Route Name | TOPICAL |
| Start Marketing Date | 20110407 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | La Prairie, Inc. |
| Substance Name | AVOBENZONE; HOMOSALATE; OCTISALATE; OXYBENZONE |
| Strength Number | 3; 7; 5; 2 |
| Strength Unit | g/100g; g/100g; g/100g; g/100g |
| Pharmaceutical Classes |
