Product NDC: | 63433-222 |
Proprietary Name: | DHC Camu Camu White Day Milk |
Non Proprietary Name: | Octinoxate and Oxybenzone |
Active Ingredient(s): | 35; 5 mg/.5mL; mg/.5mL & nbsp; Octinoxate and Oxybenzone |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 63433-222 |
Labeler Name: | DHC USA Incorporated |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20120401 |
Package NDC: | 63433-222-07 |
Package Description: | 47 mL in 1 BOTTLE, PUMP (63433-222-07) |
NDC Code | 63433-222-07 |
Proprietary Name | DHC Camu Camu White Day Milk |
Package Description | 47 mL in 1 BOTTLE, PUMP (63433-222-07) |
Product NDC | 63433-222 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Octinoxate and Oxybenzone |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20120401 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | DHC USA Incorporated |
Substance Name | OCTINOXATE; OXYBENZONE |
Strength Number | 35; 5 |
Strength Unit | mg/.5mL; mg/.5mL |
Pharmaceutical Classes |