| NDC Code | 13630-0069-4 | 
|---|
			| Package Description | 177 mL in 1 CAN (13630-0069-4) | 
|---|
			| Product NDC | 13630-0069 | 
|---|
			| Product Type Name | HUMAN OTC DRUG | 
|---|
			| Proprietary Name | Ulta | 
|---|
			| Proprietary Name Suffix | Broad Spectrum Spf 30 | 
|---|
			| Non-Proprietary Name | Avobenzone, Homosalate, Octisalate, Octocrylene And Oxybenzone | 
|---|
			| Dosage Form | SPRAY | 
|---|
			| Usage | TOPICAL | 
|---|
			| Start Marketing Date | 20031217 | 
|---|
			
			| Marketing Category Name | OTC MONOGRAPH FINAL | 
|---|
			| Application Number | part352 | 
|---|
			| Manufacturer | Prime Packaging, Inc. | 
|---|
			| Substance Name | AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE | 
|---|
			| Strength | 16.3; 22.4; 22.4; 22.4; 40.8 | 
|---|
			| Strength Unit | mg/mL; mg/mL; mg/mL; mg/mL; mg/mL | 
|---|