| Product NDC: | 10742-8368 |
| Proprietary Name: | Hada Labo Tokyo Protecting Day |
| Non Proprietary Name: | Avobenzone, Octinoxate, Octisalate, Octocrylene |
| Active Ingredient(s): | 20; 75; 25; 18 mg/mL; mg/mL; mg/mL; mg/mL & nbsp; Avobenzone, Octinoxate, Octisalate, Octocrylene |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 10742-8368 |
| Labeler Name: | The Mentholatum Company |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20130617 |
| Package NDC: | 10742-8368-1 |
| Package Description: | 1 BOTTLE in 1 CARTON (10742-8368-1) > 50 mL in 1 BOTTLE |
| NDC Code | 10742-8368-1 |
| Proprietary Name | Hada Labo Tokyo Protecting Day |
| Package Description | 1 BOTTLE in 1 CARTON (10742-8368-1) > 50 mL in 1 BOTTLE |
| Product NDC | 10742-8368 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Avobenzone, Octinoxate, Octisalate, Octocrylene |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20130617 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | The Mentholatum Company |
| Substance Name | AVOBENZONE; OCTINOXATE; OCTISALATE; OCTOCRYLENE |
| Strength Number | 20; 75; 25; 18 |
| Strength Unit | mg/mL; mg/mL; mg/mL; mg/mL |
| Pharmaceutical Classes |