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"58414-0019-1" National Drug Code (NDC)
Neostrata Enlighten Skin Brightener 1 TUBE in 1 CARTON (58414-0019-1) / 40 g in 1 TUBE
(NeoStrata Company Inc.)
NDC Code
58414-0019-1
Package Description
1 TUBE in 1 CARTON (58414-0019-1) / 40 g in 1 TUBE
Product NDC
58414-0019
Product Type Name
HUMAN OTC DRUG
Proprietary Name
Neostrata Enlighten Skin Brightener
Proprietary Name Suffix
With Sunscreen Broad Spectrum Spf 35
Non-Proprietary Name
Octinoxate, Octisalate, And Avobenzone
Dosage Form
CREAM
Usage
TOPICAL
Start Marketing Date
20181201
Marketing Category Name
OTC MONOGRAPH NOT FINAL
Application Number
part352
Manufacturer
NeoStrata Company Inc.
Substance Name
AVOBENZONE; OCTINOXATE; OCTISALATE
Strength
30; 75; 50
Strength Unit
mg/g; mg/g; mg/g
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/58414-0019-1