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sunscreen
sunscreen - 19392-300-01 - (octinoxate, oxybenzone)
Drug Information of sunscreen
| Product NDC: | 19392-300 |
| Proprietary Name: | sunscreen |
| Non Proprietary Name: | octinoxate, oxybenzone |
| Active Ingredient(s): | 75; 40 mg/g; mg/g & nbsp; octinoxate, oxybenzone |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIPSTICK |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of sunscreen
| Product NDC: | 19392-300 |
| Labeler Name: | Humphreyline |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100101 |
Package Information of sunscreen
| Package NDC: | 19392-300-01 |
| Package Description: | 4 g in 1 BOTTLE, PLASTIC (19392-300-01) |
NDC Information of sunscreen
| NDC Code | 19392-300-01 |
| Proprietary Name | sunscreen |
| Package Description | 4 g in 1 BOTTLE, PLASTIC (19392-300-01) |
| Product NDC | 19392-300 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | octinoxate, oxybenzone |
| Dosage Form Name | LIPSTICK |
| Route Name | TOPICAL |
| Start Marketing Date | 20100101 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Humphreyline |
| Substance Name | OCTINOXATE; OXYBENZONE |
| Strength Number | 75; 40 |
| Strength Unit | mg/g; mg/g |
| Pharmaceutical Classes |
