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EQUALINE
EQUALINE - 41163-356-06 - (OCTISALATE, AVOBENZONE, HOMOSALATE, OCTOCRYLENE)
Drug Information of EQUALINE
| Product NDC: | 41163-356 |
| Proprietary Name: | EQUALINE |
| Non Proprietary Name: | OCTISALATE, AVOBENZONE, HOMOSALATE, OCTOCRYLENE |
| Active Ingredient(s): | 30; 30; 50; 26 mg/mL; mg/mL; mg/mL; mg/mL & nbsp; OCTISALATE, AVOBENZONE, HOMOSALATE, OCTOCRYLENE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of EQUALINE
| Product NDC: | 41163-356 |
| Labeler Name: | SUPERVALU INC. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20130315 |
Package Information of EQUALINE
| Package NDC: | 41163-356-06 |
| Package Description: | 178 mL in 1 BOTTLE, PLASTIC (41163-356-06) |
NDC Information of EQUALINE
| NDC Code | 41163-356-06 |
| Proprietary Name | EQUALINE |
| Package Description | 178 mL in 1 BOTTLE, PLASTIC (41163-356-06) |
| Product NDC | 41163-356 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTISALATE, AVOBENZONE, HOMOSALATE, OCTOCRYLENE |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20130315 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | SUPERVALU INC. |
| Substance Name | AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE |
| Strength Number | 30; 30; 50; 26 |
| Strength Unit | mg/mL; mg/mL; mg/mL; mg/mL |
| Pharmaceutical Classes |
