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Eucerin Redness Relief Daily Perfecting
Eucerin Redness Relief Daily Perfecting - 10356-352-32 - (Octinoxate, Octisalate, Titanium Dioxide)
Drug Information of Eucerin Redness Relief Daily Perfecting
| Product NDC: | 10356-352 |
| Proprietary Name: | Eucerin Redness Relief Daily Perfecting |
| Non Proprietary Name: | Octinoxate, Octisalate, Titanium Dioxide |
| Active Ingredient(s): | 7.5; 5; 4 mL/100mL; mL/100mL; mL/100mL & nbsp; Octinoxate, Octisalate, Titanium Dioxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Eucerin Redness Relief Daily Perfecting
| Product NDC: | 10356-352 |
| Labeler Name: | Beiersdorf Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20090102 |
Package Information of Eucerin Redness Relief Daily Perfecting
| Package NDC: | 10356-352-32 |
| Package Description: | 1.5 mL in 1 PACKET (10356-352-32) |
NDC Information of Eucerin Redness Relief Daily Perfecting
| NDC Code | 10356-352-32 |
| Proprietary Name | Eucerin Redness Relief Daily Perfecting |
| Package Description | 1.5 mL in 1 PACKET (10356-352-32) |
| Product NDC | 10356-352 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Octinoxate, Octisalate, Titanium Dioxide |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20090102 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Beiersdorf Inc |
| Substance Name | OCTINOXATE; OCTISALATE; TITANIUM DIOXIDE |
| Strength Number | 7.5; 5; 4 |
| Strength Unit | mL/100mL; mL/100mL; mL/100mL |
| Pharmaceutical Classes |
