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Hydra Day SPF 20
Hydra Day SPF 20 - 76159-123-02 - (OCTINOXATE, OCTISALATE, OXYBENZONE, TITANIUM DIOXIDE)
Drug Information of Hydra Day SPF 20
| Product NDC: | 76159-123 |
| Proprietary Name: | Hydra Day SPF 20 |
| Non Proprietary Name: | OCTINOXATE, OCTISALATE, OXYBENZONE, TITANIUM DIOXIDE |
| Active Ingredient(s): | 7.5; 3; 3; .4 mL/100mL; mL/100mL; mL/100mL; mL/100mL & nbsp; OCTINOXATE, OCTISALATE, OXYBENZONE, TITANIUM DIOXIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Hydra Day SPF 20
| Product NDC: | 76159-123 |
| Labeler Name: | 3LAB, Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110415 |
Package Information of Hydra Day SPF 20
| Package NDC: | 76159-123-02 |
| Package Description: | 6 mL in 1 TUBE (76159-123-02) |
NDC Information of Hydra Day SPF 20
| NDC Code | 76159-123-02 |
| Proprietary Name | Hydra Day SPF 20 |
| Package Description | 6 mL in 1 TUBE (76159-123-02) |
| Product NDC | 76159-123 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE, OCTISALATE, OXYBENZONE, TITANIUM DIOXIDE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20110415 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | 3LAB, Inc |
| Substance Name | OCTINOXATE; OCTISALATE; OXYBENZONE; TITANIUM DIOXIDE |
| Strength Number | 7.5; 3; 3; .4 |
| Strength Unit | mL/100mL; mL/100mL; mL/100mL; mL/100mL |
| Pharmaceutical Classes |
