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"51523-772-22" National Drug Code (NDC)
Face It Aqua Uv Color Control 1 CONTAINER in 1 CARTON (51523-772-22) > 20 g in 1 CONTAINER
(THEFACESHOP CO., LTD.)
NDC Code
51523-772-22
Package Description
1 CONTAINER in 1 CARTON (51523-772-22) > 20 g in 1 CONTAINER
Product NDC
51523-772
Product Type Name
HUMAN OTC DRUG
Proprietary Name
Face It Aqua Uv Color Control
Proprietary Name Suffix
32800772
Non-Proprietary Name
Octinoxate, Titanium Dioxide And Zinc Oxide
Dosage Form
CREAM
Usage
TOPICAL
Start Marketing Date
20141120
Marketing Category Name
OTC MONOGRAPH NOT FINAL
Application Number
part352
Manufacturer
THEFACESHOP CO., LTD.
Substance Name
OCTINOXATE; TITANIUM DIOXIDE; ZINC OXIDE
Strength
.8; 2.3; .2
Strength Unit
g/20g; g/20g; g/20g
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/51523-772-22