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DAY HYDRATOR
DAY HYDRATOR - 57367-027-19 - (OCTINOXATE and OCTISALATE and OXYBENZONE)
Drug Information of DAY HYDRATOR
| Product NDC: | 57367-027 |
| Proprietary Name: | DAY HYDRATOR |
| Non Proprietary Name: | OCTINOXATE and OCTISALATE and OXYBENZONE |
| Active Ingredient(s): | 75; 50; 30 mg/g; mg/g; mg/g & nbsp; OCTINOXATE and OCTISALATE and OXYBENZONE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of DAY HYDRATOR
| Product NDC: | 57367-027 |
| Labeler Name: | 220 Laboratories Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20060201 |
Package Information of DAY HYDRATOR
| Package NDC: | 57367-027-19 |
| Package Description: | 1 TUBE in 1 CARTON (57367-027-19) > 56 g in 1 TUBE (57367-027-18) |
NDC Information of DAY HYDRATOR
| NDC Code | 57367-027-19 |
| Proprietary Name | DAY HYDRATOR |
| Package Description | 1 TUBE in 1 CARTON (57367-027-19) > 56 g in 1 TUBE (57367-027-18) |
| Product NDC | 57367-027 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE and OCTISALATE and OXYBENZONE |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20060201 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | 220 Laboratories Inc. |
| Substance Name | OCTINOXATE; OCTISALATE; OXYBENZONE |
| Strength Number | 75; 50; 30 |
| Strength Unit | mg/g; mg/g; mg/g |
| Pharmaceutical Classes |
