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SUNSCREEN MOISTURIZER
SUNSCREEN MOISTURIZER - 46007-203-21 - (AVOBENZONE OCTINOXATE OCTISALATE OXYBENZONE HOMOSALATE OCTOCRYLENE)
Drug Information of SUNSCREEN MOISTURIZER
| Product NDC: | 46007-203 |
| Proprietary Name: | SUNSCREEN MOISTURIZER |
| Non Proprietary Name: | AVOBENZONE OCTINOXATE OCTISALATE OXYBENZONE HOMOSALATE OCTOCRYLENE |
| Active Ingredient(s): | 3; 7; 7.5; 5; 3; 6 g/100mL; g/100mL; g/100mL; g/100mL; g/100mL; g/100mL & nbsp; AVOBENZONE OCTINOXATE OCTISALATE OXYBENZONE HOMOSALATE OCTOCRYLENE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SUNSCREEN MOISTURIZER
| Product NDC: | 46007-203 |
| Labeler Name: | Skin Authority LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120419 |
Package Information of SUNSCREEN MOISTURIZER
| Package NDC: | 46007-203-21 |
| Package Description: | 20 mL in 1 TUBE (46007-203-21) |
NDC Information of SUNSCREEN MOISTURIZER
| NDC Code | 46007-203-21 |
| Proprietary Name | SUNSCREEN MOISTURIZER |
| Package Description | 20 mL in 1 TUBE (46007-203-21) |
| Product NDC | 46007-203 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | AVOBENZONE OCTINOXATE OCTISALATE OXYBENZONE HOMOSALATE OCTOCRYLENE |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20120419 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Skin Authority LLC |
| Substance Name | AVOBENZONE; HOMOSALATE; OCTINOXATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE |
| Strength Number | 3; 7; 7.5; 5; 3; 6 |
| Strength Unit | g/100mL; g/100mL; g/100mL; g/100mL; g/100mL; g/100mL |
| Pharmaceutical Classes |
