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CLARINS BROAD SPECTRUM SPF 30 - SUNSCREEN CARE - 58668-4091-1 - (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE)

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Drug Information of CLARINS BROAD SPECTRUM SPF 30 - SUNSCREEN CARE

Product NDC: 58668-4091
Proprietary Name: CLARINS BROAD SPECTRUM SPF 30 - SUNSCREEN CARE
Non Proprietary Name: AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE
Active Ingredient(s): 30; 100; 50; 27; 30    mg/mL; mg/mL; mg/mL; mg/mL; mg/mL & nbsp;   AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of CLARINS BROAD SPECTRUM SPF 30 - SUNSCREEN CARE

Product NDC: 58668-4091
Labeler Name: Laboratoires Clarins S.A.
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20130508

Package Information of CLARINS BROAD SPECTRUM SPF 30 - SUNSCREEN CARE

Package NDC: 58668-4091-1
Package Description: 1 BOTTLE in 1 CARTON (58668-4091-1) > 125 mL in 1 BOTTLE

NDC Information of CLARINS BROAD SPECTRUM SPF 30 - SUNSCREEN CARE

NDC Code 58668-4091-1
Proprietary Name CLARINS BROAD SPECTRUM SPF 30 - SUNSCREEN CARE
Package Description 1 BOTTLE in 1 CARTON (58668-4091-1) > 125 mL in 1 BOTTLE
Product NDC 58668-4091
Product Type Name HUMAN OTC DRUG
Non Proprietary Name AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20130508
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Laboratoires Clarins S.A.
Substance Name AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE
Strength Number 30; 100; 50; 27; 30
Strength Unit mg/mL; mg/mL; mg/mL; mg/mL; mg/mL
Pharmaceutical Classes

Complete Information of CLARINS BROAD SPECTRUM SPF 30 - SUNSCREEN CARE


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