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"83866-6202-2" National Drug Code (NDC)

Omnilux Mineral Facial Sunscreen 1 BOTTLE, PUMP in 1 CARTON (83866-6202-2) / 50 mL in 1 BOTTLE, PUMP (83866-6202-1)
(The Lotus Global Group, Inc, dba GlobalMed Technologies)

NDC Code83866-6202-2
Package Description1 BOTTLE, PUMP in 1 CARTON (83866-6202-2) / 50 mL in 1 BOTTLE, PUMP (83866-6202-1)
Product NDC83866-6202
Product Type NameHUMAN OTC DRUG
Proprietary NameOmnilux Mineral Facial Sunscreen
Non-Proprietary NameZinc Oxide
Dosage FormLOTION
UsageTOPICAL
Start Marketing Date20240726
Marketing Category NameOTC MONOGRAPH DRUG
Application NumberM020
ManufacturerThe Lotus Global Group, Inc, dba GlobalMed Technologies
Substance NameZINC OXIDE
Strength132
Strength Unitmg/mL

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/83866-6202-2





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