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Guerlain Super Aqua-Day
Guerlain Super Aqua-Day - 49817-0021-1 - (OCTINOXATE, OXYBENZONE, TITANIUM DIOXIDE, OCTOCRYLENE, SULISOBENZONE)
Drug Information of Guerlain Super Aqua-Day
| Product NDC: | 49817-0021 |
| Proprietary Name: | Guerlain Super Aqua-Day |
| Non Proprietary Name: | OCTINOXATE, OXYBENZONE, TITANIUM DIOXIDE, OCTOCRYLENE, SULISOBENZONE |
| Active Ingredient(s): | 7.4; 2; 3; .5; 2.4 mL/100mL; mL/100mL; mL/100mL; mL/100mL; mL/100mL & nbsp; OCTINOXATE, OXYBENZONE, TITANIUM DIOXIDE, OCTOCRYLENE, SULISOBENZONE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Guerlain Super Aqua-Day
| Product NDC: | 49817-0021 |
| Labeler Name: | Guerlain S.A. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100617 |
Package Information of Guerlain Super Aqua-Day
| Package NDC: | 49817-0021-1 |
| Package Description: | 40 mL in 1 BOTTLE (49817-0021-1) |
NDC Information of Guerlain Super Aqua-Day
| NDC Code | 49817-0021-1 |
| Proprietary Name | Guerlain Super Aqua-Day |
| Package Description | 40 mL in 1 BOTTLE (49817-0021-1) |
| Product NDC | 49817-0021 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE, OXYBENZONE, TITANIUM DIOXIDE, OCTOCRYLENE, SULISOBENZONE |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20100617 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Guerlain S.A. |
| Substance Name | OCTINOXATE; OCTOCRYLENE; OXYBENZONE; SULISOBENZONE; TITANIUM DIOXIDE |
| Strength Number | 7.4; 2; 3; .5; 2.4 |
| Strength Unit | mL/100mL; mL/100mL; mL/100mL; mL/100mL; mL/100mL |
| Pharmaceutical Classes |
