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Suntan Lotion - 49852-200-60 - (OCTINOXATE OXYBENZONE TITANIUM DIOXIDE)

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Drug Information of Suntan Lotion

Product NDC: 49852-200
Proprietary Name: Suntan Lotion
Non Proprietary Name: OCTINOXATE OXYBENZONE TITANIUM DIOXIDE
Active Ingredient(s): 7; 6; 1    mL/100mL; mL/100mL; mL/100mL & nbsp;   OCTINOXATE OXYBENZONE TITANIUM DIOXIDE
Administration Route(s): TOPICAL
Dosage Form(s): LOTION
Coding System: National Drug Codes(NDC)

Labeler Information of Suntan Lotion

Product NDC: 49852-200
Labeler Name: Tri-Coastal Design Company Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20100228

Package Information of Suntan Lotion

Package NDC: 49852-200-60
Package Description: 60 mL in 1 TUBE (49852-200-60)

NDC Information of Suntan Lotion

NDC Code 49852-200-60
Proprietary Name Suntan Lotion
Package Description 60 mL in 1 TUBE (49852-200-60)
Product NDC 49852-200
Product Type Name HUMAN OTC DRUG
Non Proprietary Name OCTINOXATE OXYBENZONE TITANIUM DIOXIDE
Dosage Form Name LOTION
Route Name TOPICAL
Start Marketing Date 20100228
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Tri-Coastal Design Company Inc.
Substance Name OCTINOXATE; OXYBENZONE; TITANIUM DIOXIDE
Strength Number 7; 6; 1
Strength Unit mL/100mL; mL/100mL; mL/100mL
Pharmaceutical Classes

Complete Information of Suntan Lotion


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