www.ndcvalidator.com
National Drug Code Lookup
|
NDC Directory
|
About
|
Feedback
"51785-086-20" National Drug Code (NDC)
Skin Activator Day 1 TUBE in 1 CARTON (51785-086-20) > 50 mL in 1 TUBE
(Herbalife International of America, Inc.)
NDC Code
51785-086-20
Package Description
1 TUBE in 1 CARTON (51785-086-20) > 50 mL in 1 TUBE
Product NDC
51785-086
Product Type Name
HUMAN OTC DRUG
Proprietary Name
Skin Activator Day
Proprietary Name Suffix
Spf 15
Non-Proprietary Name
Octinoxate, Octisalate And Avobenzone
Dosage Form
LOTION
Usage
TOPICAL
Start Marketing Date
20111021
Marketing Category Name
OTC MONOGRAPH NOT FINAL
Application Number
part352
Manufacturer
Herbalife International of America, Inc.
Substance Name
OCTINOXATE; OCTISALATE; AVOBENZONE
Strength
.0742; .0495; .0198
Strength Unit
g/mL; g/mL; g/mL
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/51785-086-20