 
                        | Product NDC: | 42315-672 | 
| Proprietary Name: | moisturising sunscreen | 
| Non Proprietary Name: | Homosalate, Octisalate, Octinoxate, Octocrylene | 
| Active Ingredient(s): | 8; 3; 4 mL/100mL; mL/100mL; mL/100mL & nbsp; Homosalate, Octisalate, Octinoxate, Octocrylene | 
| Administration Route(s): | TOPICAL | 
| Dosage Form(s): | CREAM | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 42315-672 | 
| Labeler Name: | Eshu Pty Ltd | 
| Product Type: | HUMAN OTC DRUG | 
| FDA Application Number: | part352 | 
| Marketing Category: | OTC MONOGRAPH NOT FINAL | 
| Start Marketing Date: | 20110217 | 
| Package NDC: | 42315-672-02 | 
| Package Description: | 1 BOTTLE in 1 BOX (42315-672-02) > 100 mL in 1 BOTTLE (42315-672-01) | 
| NDC Code | 42315-672-02 | 
| Proprietary Name | moisturising sunscreen | 
| Package Description | 1 BOTTLE in 1 BOX (42315-672-02) > 100 mL in 1 BOTTLE (42315-672-01) | 
| Product NDC | 42315-672 | 
| Product Type Name | HUMAN OTC DRUG | 
| Non Proprietary Name | Homosalate, Octisalate, Octinoxate, Octocrylene | 
| Dosage Form Name | CREAM | 
| Route Name | TOPICAL | 
| Start Marketing Date | 20110217 | 
| Marketing Category Name | OTC MONOGRAPH NOT FINAL | 
| Labeler Name | Eshu Pty Ltd | 
| Substance Name | HOMOSALATE; OCTINOXATE; OCTISALATE | 
| Strength Number | 8; 3; 4 | 
| Strength Unit | mL/100mL; mL/100mL; mL/100mL | 
| Pharmaceutical Classes |