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"58414-0011-1" National Drug Code (NDC)
Neostrata Enlighten Skin Brightener 1 TUBE in 1 CARTON (58414-0011-1) > 40 g in 1 TUBE
(NeoStrata Company Inc.)
NDC Code
58414-0011-1
Package Description
1 TUBE in 1 CARTON (58414-0011-1) > 40 g in 1 TUBE
Product NDC
58414-0011
Product Type Name
HUMAN OTC DRUG
Proprietary Name
Neostrata Enlighten Skin Brightener
Proprietary Name Suffix
Spf 25
Non-Proprietary Name
Octinoxate, Octisalate, And Avobenzone
Dosage Form
CREAM
Usage
TOPICAL
Start Marketing Date
20151001
End Marketing Date
20210731
Marketing Category Name
OTC MONOGRAPH NOT FINAL
Application Number
part352
Manufacturer
NeoStrata Company Inc.
Substance Name
OCTINOXATE; OCTISALATE; AVOBENZONE
Strength
75; 50; 30
Strength Unit
mg/g; mg/g; mg/g
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/58414-0011-1