Product NDC: | 49817-0022 |
Proprietary Name: | Guerlain Super Aqua-Hands |
Non Proprietary Name: | OCTINOXATE, OXYBENZONE, AVOBENZONE |
Active Ingredient(s): | .5; 7.4; 2.5 mL/100mL; mL/100mL; mL/100mL & nbsp; OCTINOXATE, OXYBENZONE, AVOBENZONE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 49817-0022 |
Labeler Name: | Guerlain S.A. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20100714 |
Package NDC: | 49817-0022-2 |
Package Description: | 75 mL in 1 TUBE (49817-0022-2) |
NDC Code | 49817-0022-2 |
Proprietary Name | Guerlain Super Aqua-Hands |
Package Description | 75 mL in 1 TUBE (49817-0022-2) |
Product NDC | 49817-0022 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | OCTINOXATE, OXYBENZONE, AVOBENZONE |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20100714 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Guerlain S.A. |
Substance Name | AVOBENZONE; OCTINOXATE; OXYBENZONE |
Strength Number | .5; 7.4; 2.5 |
Strength Unit | mL/100mL; mL/100mL; mL/100mL |
Pharmaceutical Classes |