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TECHNIblock ULTRA SUNSCREEN - 49672-100-01 - (AVOBENZONE,OCTINOXATE,OXYBENZONE,PADIMATE)

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Drug Information of TECHNIblock ULTRA SUNSCREEN

Product NDC: 49672-100
Proprietary Name: TECHNIblock ULTRA SUNSCREEN
Non Proprietary Name: AVOBENZONE,OCTINOXATE,OXYBENZONE,PADIMATE
Active Ingredient(s): .6; 6.3; 3.4; 5.1    mL/100mL; mL/100mL; mL/100mL; mL/100mL & nbsp;   AVOBENZONE,OCTINOXATE,OXYBENZONE,PADIMATE
Administration Route(s): TOPICAL
Dosage Form(s): LOTION
Coding System: National Drug Codes(NDC)

Labeler Information of TECHNIblock ULTRA SUNSCREEN

Product NDC: 49672-100
Labeler Name: The Myles Group LLC
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20100405

Package Information of TECHNIblock ULTRA SUNSCREEN

Package NDC: 49672-100-01
Package Description: 125 mL in 1 PACKAGE (49672-100-01)

NDC Information of TECHNIblock ULTRA SUNSCREEN

NDC Code 49672-100-01
Proprietary Name TECHNIblock ULTRA SUNSCREEN
Package Description 125 mL in 1 PACKAGE (49672-100-01)
Product NDC 49672-100
Product Type Name HUMAN OTC DRUG
Non Proprietary Name AVOBENZONE,OCTINOXATE,OXYBENZONE,PADIMATE
Dosage Form Name LOTION
Route Name TOPICAL
Start Marketing Date 20100405
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name The Myles Group LLC
Substance Name AVOBENZONE; OCTINOXATE; OXYBENZONE; PADIMATE A
Strength Number .6; 6.3; 3.4; 5.1
Strength Unit mL/100mL; mL/100mL; mL/100mL; mL/100mL
Pharmaceutical Classes

Complete Information of TECHNIblock ULTRA SUNSCREEN


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