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glytone retexturize body
glytone retexturize body - 64760-208-01 - (octinoxate, octisalate, oxybenzone)
Drug Information of glytone retexturize body
| Product NDC: | 64760-208 |
| Proprietary Name: | glytone retexturize body |
| Non Proprietary Name: | octinoxate, octisalate, oxybenzone |
| Active Ingredient(s): | 18.75; 12.5; 7.5 mL/250mL; mL/250mL; mL/250mL & nbsp; octinoxate, octisalate, oxybenzone |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of glytone retexturize body
| Product NDC: | 64760-208 |
| Labeler Name: | Glytone |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100519 |
Package Information of glytone retexturize body
| Package NDC: | 64760-208-01 |
| Package Description: | 1 BOTTLE in 1 BOX (64760-208-01) > 250 mL in 1 BOTTLE |
NDC Information of glytone retexturize body
| NDC Code | 64760-208-01 |
| Proprietary Name | glytone retexturize body |
| Package Description | 1 BOTTLE in 1 BOX (64760-208-01) > 250 mL in 1 BOTTLE |
| Product NDC | 64760-208 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | octinoxate, octisalate, oxybenzone |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20100519 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Glytone |
| Substance Name | OCTINOXATE; OCTISALATE; OXYBENZONE |
| Strength Number | 18.75; 12.5; 7.5 |
| Strength Unit | mL/250mL; mL/250mL; mL/250mL |
| Pharmaceutical Classes |
