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Aloe Sunscreen - 11697-199-04 - (Homosalate)

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Drug Information of Aloe Sunscreen

Product NDC: 11697-199
Proprietary Name: Aloe Sunscreen
Non Proprietary Name: Homosalate
Active Ingredient(s): 3.54; 3.54; 1.18; 5.9; 3.922    mL/118mL; mL/118mL; mL/118mL; mL/118mL; mL/118mL & nbsp;   Homosalate
Administration Route(s): TOPICAL
Dosage Form(s): LOTION
Coding System: National Drug Codes(NDC)

Labeler Information of Aloe Sunscreen

Product NDC: 11697-199
Labeler Name: Aloe Vera of America, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20110406

Package Information of Aloe Sunscreen

Package NDC: 11697-199-04
Package Description: 118 mL in 1 TUBE (11697-199-04)

NDC Information of Aloe Sunscreen

NDC Code 11697-199-04
Proprietary Name Aloe Sunscreen
Package Description 118 mL in 1 TUBE (11697-199-04)
Product NDC 11697-199
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Homosalate
Dosage Form Name LOTION
Route Name TOPICAL
Start Marketing Date 20110406
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Aloe Vera of America, Inc.
Substance Name AVOBENZONE; ENSULIZOLE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
Strength Number 3.54; 3.54; 1.18; 5.9; 3.922
Strength Unit mL/118mL; mL/118mL; mL/118mL; mL/118mL; mL/118mL
Pharmaceutical Classes

Complete Information of Aloe Sunscreen


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