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glytone retexturize hand
glytone retexturize hand - 64760-207-01 - (octinoxate, octisalate, oxybenzone)
Drug Information of glytone retexturize hand
| Product NDC: | 64760-207 |
| Proprietary Name: | glytone retexturize hand |
| Non Proprietary Name: | octinoxate, octisalate, oxybenzone |
| Active Ingredient(s): | 7.2; 3.6; 6 mm/120mL; mL/120mL; mL/120mL & nbsp; octinoxate, octisalate, oxybenzone |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of glytone retexturize hand
| Product NDC: | 64760-207 |
| Labeler Name: | Genesis Pharmaceuticals |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100524 |
Package Information of glytone retexturize hand
| Package NDC: | 64760-207-01 |
| Package Description: | 120 mL in 1 TUBE (64760-207-01) |
NDC Information of glytone retexturize hand
| NDC Code | 64760-207-01 |
| Proprietary Name | glytone retexturize hand |
| Package Description | 120 mL in 1 TUBE (64760-207-01) |
| Product NDC | 64760-207 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | octinoxate, octisalate, oxybenzone |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20100524 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Genesis Pharmaceuticals |
| Substance Name | OCTINOXATE; OCTISALATE; OXYBENZONE |
| Strength Number | 7.2; 3.6; 6 |
| Strength Unit | mm/120mL; mL/120mL; mL/120mL |
| Pharmaceutical Classes |
