| 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 |