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"71644-004-50" National Drug Code (NDC)
Cyberderm 1 BOTTLE in 1 CARTON (71644-004-50) > 50 mL in 1 BOTTLE
(Cyberderm Laboratories Inc.)
NDC Code
71644-004-50
Package Description
1 BOTTLE in 1 CARTON (71644-004-50) > 50 mL in 1 BOTTLE
Product NDC
71644-004
Product Type Name
HUMAN OTC DRUG
Proprietary Name
Cyberderm
Proprietary Name Suffix
Every Morning Sun Whip
Non-Proprietary Name
Zinc Oxide, Octinoxate
Dosage Form
LOTION
Usage
TOPICAL
Start Marketing Date
20180330
Marketing Category Name
OTC MONOGRAPH FINAL
Application Number
part352
Manufacturer
Cyberderm Laboratories Inc.
Substance Name
OCTINOXATE; ZINC OXIDE
Strength
7.5; 15
Strength Unit
g/100mL; g/100mL
Pharmacy Classes
Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/71644-004-50