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Rite Aid Sunscreen - 11822-9014-9 - (OCTINOXATE, OCTISALATE, OXYBENZONE)

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Drug Information of Rite Aid Sunscreen

Product NDC: 11822-9014
Proprietary Name: Rite Aid Sunscreen
Non Proprietary Name: OCTINOXATE, OCTISALATE, OXYBENZONE
Active Ingredient(s): 7.5; 5; 6    g/100g; g/100g; g/100g & nbsp;   OCTINOXATE, OCTISALATE, OXYBENZONE
Administration Route(s): TOPICAL
Dosage Form(s): LOTION
Coding System: National Drug Codes(NDC)

Labeler Information of Rite Aid Sunscreen

Product NDC: 11822-9014
Labeler Name: RITE AID CORPORATION
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20121205

Package Information of Rite Aid Sunscreen

Package NDC: 11822-9014-9
Package Description: 453 g in 1 BOTTLE, PLASTIC (11822-9014-9)

NDC Information of Rite Aid Sunscreen

NDC Code 11822-9014-9
Proprietary Name Rite Aid Sunscreen
Package Description 453 g in 1 BOTTLE, PLASTIC (11822-9014-9)
Product NDC 11822-9014
Product Type Name HUMAN OTC DRUG
Non Proprietary Name OCTINOXATE, OCTISALATE, OXYBENZONE
Dosage Form Name LOTION
Route Name TOPICAL
Start Marketing Date 20121205
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name RITE AID CORPORATION
Substance Name OCTINOXATE; OCTISALATE; OXYBENZONE
Strength Number 7.5; 5; 6
Strength Unit g/100g; g/100g; g/100g
Pharmaceutical Classes

Complete Information of Rite Aid Sunscreen


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