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Sun-Kissed Lip Balm
Sun-Kissed Lip Balm - 75862-015-50 - (OCTINOXATE, OCTOCRYLENE, OCTISALATE, and OXYBENZONE)
Drug Information of Sun-Kissed Lip Balm
| Product NDC: | 75862-015 |
| Proprietary Name: | Sun-Kissed Lip Balm |
| Non Proprietary Name: | OCTINOXATE, OCTOCRYLENE, OCTISALATE, and OXYBENZONE |
| Active Ingredient(s): | 7.5; 5; 7; 5 g/100g; g/100g; g/100g; g/100g & nbsp; OCTINOXATE, OCTOCRYLENE, OCTISALATE, and OXYBENZONE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | STICK |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sun-Kissed Lip Balm
| Product NDC: | 75862-015 |
| Labeler Name: | GANZ U.S.A., LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110101 |
Package Information of Sun-Kissed Lip Balm
| Package NDC: | 75862-015-50 |
| Package Description: | 1 TUBE in 1 BOX (75862-015-50) > 4 g in 1 TUBE |
NDC Information of Sun-Kissed Lip Balm
| NDC Code | 75862-015-50 |
| Proprietary Name | Sun-Kissed Lip Balm |
| Package Description | 1 TUBE in 1 BOX (75862-015-50) > 4 g in 1 TUBE |
| Product NDC | 75862-015 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE, OCTOCRYLENE, OCTISALATE, and OXYBENZONE |
| Dosage Form Name | STICK |
| Route Name | TOPICAL |
| Start Marketing Date | 20110101 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | GANZ U.S.A., LLC |
| Substance Name | OCTINOXATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE |
| Strength Number | 7.5; 5; 7; 5 |
| Strength Unit | g/100g; g/100g; g/100g; g/100g |
| Pharmaceutical Classes |
