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JAFRA PRO FACE LIFT - 68828-049-11 - (OCTOCRYLENE OCTISALATE HOMOSALATE AVOBENZONE)

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Drug Information of JAFRA PRO FACE LIFT

Product NDC: 68828-049
Proprietary Name: JAFRA PRO FACE LIFT
Non Proprietary Name: OCTOCRYLENE OCTISALATE HOMOSALATE AVOBENZONE
Active Ingredient(s): 3; 5; 5; 7    g/100mL; g/100mL; g/100mL; g/100mL & nbsp;   OCTOCRYLENE OCTISALATE HOMOSALATE AVOBENZONE
Administration Route(s): TOPICAL
Dosage Form(s): LOTION
Coding System: National Drug Codes(NDC)

Labeler Information of JAFRA PRO FACE LIFT

Product NDC: 68828-049
Labeler Name: JAFRA COSMETICS INTERNATIONAL
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20120504

Package Information of JAFRA PRO FACE LIFT

Package NDC: 68828-049-11
Package Description: 1 BOTTLE in 1 BOX (68828-049-11) > 30 mL in 1 BOTTLE (68828-049-67)

NDC Information of JAFRA PRO FACE LIFT

NDC Code 68828-049-11
Proprietary Name JAFRA PRO FACE LIFT
Package Description 1 BOTTLE in 1 BOX (68828-049-11) > 30 mL in 1 BOTTLE (68828-049-67)
Product NDC 68828-049
Product Type Name HUMAN OTC DRUG
Non Proprietary Name OCTOCRYLENE OCTISALATE HOMOSALATE AVOBENZONE
Dosage Form Name LOTION
Route Name TOPICAL
Start Marketing Date 20120504
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name JAFRA COSMETICS INTERNATIONAL
Substance Name AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
Strength Number 3; 5; 5; 7
Strength Unit g/100mL; g/100mL; g/100mL; g/100mL
Pharmaceutical Classes

Complete Information of JAFRA PRO FACE LIFT


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