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Aruba Aloe Very Water Resistant Sunscreen - 53675-158-08 - (OCTOCRYLENE, OCTINOXATE, OXYBENZONE, HOMOSALATE, OCTYL SALICYLATE, AVOBENZONE)

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Drug Information of Aruba Aloe Very Water Resistant Sunscreen

Product NDC: 53675-158
Proprietary Name: Aruba Aloe Very Water Resistant Sunscreen
Non Proprietary Name: OCTOCRYLENE, OCTINOXATE, OXYBENZONE, HOMOSALATE, OCTYL SALICYLATE, AVOBENZONE
Active Ingredient(s): 30; 50; 75; 50; 100; 60    mg/mL; mg/mL; mg/mL; mg/mL; mg/mL; mg/mL & nbsp;   OCTOCRYLENE, OCTINOXATE, OXYBENZONE, HOMOSALATE, OCTYL SALICYLATE, AVOBENZONE
Administration Route(s): TOPICAL
Dosage Form(s): LOTION
Coding System: National Drug Codes(NDC)

Labeler Information of Aruba Aloe Very Water Resistant Sunscreen

Product NDC: 53675-158
Labeler Name: Aruba Aloe Balm NV
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20130226

Package Information of Aruba Aloe Very Water Resistant Sunscreen

Package NDC: 53675-158-08
Package Description: 251 mL in 1 BOTTLE (53675-158-08)

NDC Information of Aruba Aloe Very Water Resistant Sunscreen

NDC Code 53675-158-08
Proprietary Name Aruba Aloe Very Water Resistant Sunscreen
Package Description 251 mL in 1 BOTTLE (53675-158-08)
Product NDC 53675-158
Product Type Name HUMAN OTC DRUG
Non Proprietary Name OCTOCRYLENE, OCTINOXATE, OXYBENZONE, HOMOSALATE, OCTYL SALICYLATE, AVOBENZONE
Dosage Form Name LOTION
Route Name TOPICAL
Start Marketing Date 20130226
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Aruba Aloe Balm NV
Substance Name AVOBENZONE; HOMOSALATE; OCTINOXATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE
Strength Number 30; 50; 75; 50; 100; 60
Strength Unit mg/mL; mg/mL; mg/mL; mg/mL; mg/mL; mg/mL
Pharmaceutical Classes

Complete Information of Aruba Aloe Very Water Resistant Sunscreen


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