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Sunscreen
Sunscreen - 61010-6103-1 - (Homosalate, Octinoxate, Octisalate, Oxybenzone)
Drug Information of Sunscreen
| Product NDC: | 61010-6103 |
| Proprietary Name: | Sunscreen |
| Non Proprietary Name: | Homosalate, Octinoxate, Octisalate, Oxybenzone |
| Active Ingredient(s): | 6; 7.5; 5; 5 mg/g; mg/g; mg/g; mg/g & nbsp; Homosalate, Octinoxate, Octisalate, Oxybenzone |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sunscreen
| Product NDC: | 61010-6103 |
| Labeler Name: | Safetec of America, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20070313 |
Package Information of Sunscreen
| Package NDC: | 61010-6103-1 |
| Package Description: | 25 PACKET in 1 BOX (61010-6103-1) > 3.5 g in 1 PACKET (61010-6103-0) |
NDC Information of Sunscreen
| NDC Code | 61010-6103-1 |
| Proprietary Name | Sunscreen |
| Package Description | 25 PACKET in 1 BOX (61010-6103-1) > 3.5 g in 1 PACKET (61010-6103-0) |
| Product NDC | 61010-6103 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Homosalate, Octinoxate, Octisalate, Oxybenzone |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20070313 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Safetec of America, Inc. |
| Substance Name | HOMOSALATE; OCTINOXATE; OCTISALATE; OXYBENZONE |
| Strength Number | 6; 7.5; 5; 5 |
| Strength Unit | mg/g; mg/g; mg/g; mg/g |
| Pharmaceutical Classes |
