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Cetaphil DermaControl SPF 30 - 0299-3913-01 - (octocrylene, octisalate, avobenzone)

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Drug Information of Cetaphil DermaControl SPF 30

Product NDC: 0299-3913
Proprietary Name: Cetaphil DermaControl SPF 30
Non Proprietary Name: octocrylene, octisalate, avobenzone
Active Ingredient(s): 3; 5; 7    mL/100mL; mL/100mL; mL/100mL & nbsp;   octocrylene, octisalate, avobenzone
Administration Route(s): TOPICAL
Dosage Form(s): LOTION
Coding System: National Drug Codes(NDC)

Labeler Information of Cetaphil DermaControl SPF 30

Product NDC: 0299-3913
Labeler Name: Galderma Laboratories, L.P.
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20111201

Package Information of Cetaphil DermaControl SPF 30

Package NDC: 0299-3913-01
Package Description: 7 mL in 1 TUBE (0299-3913-01)

NDC Information of Cetaphil DermaControl SPF 30

NDC Code 0299-3913-01
Proprietary Name Cetaphil DermaControl SPF 30
Package Description 7 mL in 1 TUBE (0299-3913-01)
Product NDC 0299-3913
Product Type Name HUMAN OTC DRUG
Non Proprietary Name octocrylene, octisalate, avobenzone
Dosage Form Name LOTION
Route Name TOPICAL
Start Marketing Date 20111201
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Galderma Laboratories, L.P.
Substance Name AVOBENZONE; OCTISALATE; OCTOCRYLENE
Strength Number 3; 5; 7
Strength Unit mL/100mL; mL/100mL; mL/100mL
Pharmaceutical Classes

Complete Information of Cetaphil DermaControl SPF 30


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