Product NDC: | 51523-101 |
Proprietary Name: | NATURAL SUN AQ BODY AND FAMILY MILD SUN MILK |
Non Proprietary Name: | OCTINOXATE, OCTISALATE, TITANIUM DIOXIDE, AVOBENZONE, ENZACAMENE |
Active Ingredient(s): | 2.3; 2; 7.5; 3; 2.34 mL/100mL; mL/100mL; mL/100mL; mL/100mL; mL/100mL & nbsp; OCTINOXATE, OCTISALATE, TITANIUM DIOXIDE, AVOBENZONE, ENZACAMENE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 51523-101 |
Labeler Name: | THEFACESHOP CO., LTD |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20101122 |
Package NDC: | 51523-101-02 |
Package Description: | 1 CONTAINER in 1 BOX (51523-101-02) > 120 mL in 1 CONTAINER (51523-101-01) |
NDC Code | 51523-101-02 |
Proprietary Name | NATURAL SUN AQ BODY AND FAMILY MILD SUN MILK |
Package Description | 1 CONTAINER in 1 BOX (51523-101-02) > 120 mL in 1 CONTAINER (51523-101-01) |
Product NDC | 51523-101 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | OCTINOXATE, OCTISALATE, TITANIUM DIOXIDE, AVOBENZONE, ENZACAMENE |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20101122 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | THEFACESHOP CO., LTD |
Substance Name | AVOBENZONE; ENZACAMENE; OCTINOXATE; OCTISALATE; TITANIUM DIOXIDE |
Strength Number | 2.3; 2; 7.5; 3; 2.34 |
Strength Unit | mL/100mL; mL/100mL; mL/100mL; mL/100mL; mL/100mL |
Pharmaceutical Classes |