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SUNTINTS
SUNTINTS - 40046-0034-1 - (OCTINOXATE, OCTISALATE, AVOBENZONE, HOMOSALATE, OCTOCRYLENE)
Drug Information of SUNTINTS
| Product NDC: | 40046-0034 |
| Proprietary Name: | SUNTINTS |
| Non Proprietary Name: | OCTINOXATE, OCTISALATE, AVOBENZONE, HOMOSALATE, OCTOCRYLENE |
| Active Ingredient(s): | 3; 2.9; 7.5; 5; 2.7 mL/100mL; mL/100mL; mL/100mL; mL/100mL; mL/100mL & nbsp; OCTINOXATE, OCTISALATE, AVOBENZONE, HOMOSALATE, OCTOCRYLENE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIPSTICK |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SUNTINTS
| Product NDC: | 40046-0034 |
| Labeler Name: | MAKEUP ART COSMETICS |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20091201 |
Package Information of SUNTINTS
| Package NDC: | 40046-0034-1 |
| Package Description: | 1 VIAL in 1 CARTON (40046-0034-1) > 10 mL in 1 VIAL (40046-0034-2) |
NDC Information of SUNTINTS
| NDC Code | 40046-0034-1 |
| Proprietary Name | SUNTINTS |
| Package Description | 1 VIAL in 1 CARTON (40046-0034-1) > 10 mL in 1 VIAL (40046-0034-2) |
| Product NDC | 40046-0034 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE, OCTISALATE, AVOBENZONE, HOMOSALATE, OCTOCRYLENE |
| Dosage Form Name | LIPSTICK |
| Route Name | TOPICAL |
| Start Marketing Date | 20091201 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | MAKEUP ART COSMETICS |
| Substance Name | AVOBENZONE; HOMOSALATE; OCTINOXATE; OCTISALATE; OCTOCRYLENE |
| Strength Number | 3; 2.9; 7.5; 5; 2.7 |
| Strength Unit | mL/100mL; mL/100mL; mL/100mL; mL/100mL; mL/100mL |
| Pharmaceutical Classes |
