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Hawaiian Tropic Baby - 23667-000-01 - (OCTOCRYLENE, OXYBENZONE)

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Drug Information of Hawaiian Tropic Baby

Product NDC: 23667-000
Proprietary Name: Hawaiian Tropic Baby
Non Proprietary Name: OCTOCRYLENE, OXYBENZONE
Active Ingredient(s): 8; 3.5    mL/100mL; mL/100mL & nbsp;   OCTOCRYLENE, OXYBENZONE
Administration Route(s): TOPICAL
Dosage Form(s): LOTION
Coding System: National Drug Codes(NDC)

Labeler Information of Hawaiian Tropic Baby

Product NDC: 23667-000
Labeler Name: Formulated Solutions
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20100726

Package Information of Hawaiian Tropic Baby

Package NDC: 23667-000-01
Package Description: 177 mL in 1 BOTTLE (23667-000-01)

NDC Information of Hawaiian Tropic Baby

NDC Code 23667-000-01
Proprietary Name Hawaiian Tropic Baby
Package Description 177 mL in 1 BOTTLE (23667-000-01)
Product NDC 23667-000
Product Type Name HUMAN OTC DRUG
Non Proprietary Name OCTOCRYLENE, OXYBENZONE
Dosage Form Name LOTION
Route Name TOPICAL
Start Marketing Date 20100726
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Formulated Solutions
Substance Name OCTOCRYLENE; OXYBENZONE
Strength Number 8; 3.5
Strength Unit mL/100mL; mL/100mL
Pharmaceutical Classes

Complete Information of Hawaiian Tropic Baby


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