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SENSE Daytime Protective Broad Spectrum SPF 15
SENSE Daytime Protective Broad Spectrum SPF 15 - 51861-010-00 - (OCTINOXATE, OXYBENZONE, AVOBENZONE)
Drug Information of SENSE Daytime Protective Broad Spectrum SPF 15
| Product NDC: | 51861-010 |
| Proprietary Name: | SENSE Daytime Protective Broad Spectrum SPF 15 |
| Non Proprietary Name: | OCTINOXATE, OXYBENZONE, AVOBENZONE |
| Active Ingredient(s): | 2; 7.5; 3 mL/100mL; mL/100mL; mL/100mL & nbsp; OCTINOXATE, OXYBENZONE, AVOBENZONE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | EMULSION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SENSE Daytime Protective Broad Spectrum SPF 15
| Product NDC: | 51861-010 |
| Labeler Name: | USANA Health Sciences, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120328 |
Package Information of SENSE Daytime Protective Broad Spectrum SPF 15
| Package NDC: | 51861-010-00 |
| Package Description: | 38 mL in 1 BOTTLE (51861-010-00) |
NDC Information of SENSE Daytime Protective Broad Spectrum SPF 15
| NDC Code | 51861-010-00 |
| Proprietary Name | SENSE Daytime Protective Broad Spectrum SPF 15 |
| Package Description | 38 mL in 1 BOTTLE (51861-010-00) |
| Product NDC | 51861-010 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE, OXYBENZONE, AVOBENZONE |
| Dosage Form Name | EMULSION |
| Route Name | TOPICAL |
| Start Marketing Date | 20120328 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | USANA Health Sciences, Inc. |
| Substance Name | AVOBENZONE; OCTINOXATE; OXYBENZONE |
| Strength Number | 2; 7.5; 3 |
| Strength Unit | mL/100mL; mL/100mL; mL/100mL |
| Pharmaceutical Classes |
