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Sun Defeated Sunscreen
Sun Defeated Sunscreen - 51702-114-02 - (Avobenzone, Octocrylene, Oxybenzone, Octisalate)
Drug Information of Sun Defeated Sunscreen
| Product NDC: | 51702-114 |
| Proprietary Name: | Sun Defeated Sunscreen |
| Non Proprietary Name: | Avobenzone, Octocrylene, Oxybenzone, Octisalate |
| Active Ingredient(s): | 2.79; 7.44; 6.51; 3.74 g/93g; g/93g; g/93g; g/93g & nbsp; Avobenzone, Octocrylene, Oxybenzone, Octisalate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sun Defeated Sunscreen
| Product NDC: | 51702-114 |
| Labeler Name: | Mission |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120312 |
Package Information of Sun Defeated Sunscreen
| Package NDC: | 51702-114-02 |
| Package Description: | 1 TUBE in 1 BOX (51702-114-02) > 93 g in 1 TUBE (51702-114-01) |
NDC Information of Sun Defeated Sunscreen
| NDC Code | 51702-114-02 |
| Proprietary Name | Sun Defeated Sunscreen |
| Package Description | 1 TUBE in 1 BOX (51702-114-02) > 93 g in 1 TUBE (51702-114-01) |
| Product NDC | 51702-114 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Avobenzone, Octocrylene, Oxybenzone, Octisalate |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20120312 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Mission |
| Substance Name | AVOBENZONE; OCTISALATE; OCTOCRYLENE; OXYBENZONE |
| Strength Number | 2.79; 7.44; 6.51; 3.74 |
| Strength Unit | g/93g; g/93g; g/93g; g/93g |
| Pharmaceutical Classes |
