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BAEKNYONDONGAN TREATMENT - 54948-100-01 - (WITCH HAZEL)

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Drug Information of BAEKNYONDONGAN TREATMENT

Product NDC: 54948-100
Proprietary Name: BAEKNYONDONGAN TREATMENT
Non Proprietary Name: WITCH HAZEL
Active Ingredient(s): .55    mL/550mL & nbsp;   WITCH HAZEL
Administration Route(s): TOPICAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of BAEKNYONDONGAN TREATMENT

Product NDC: 54948-100
Labeler Name: MIX & MATCH CO., LTD.
Product Type: HUMAN OTC DRUG
FDA Application Number: part347
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20110803

Package Information of BAEKNYONDONGAN TREATMENT

Package NDC: 54948-100-01
Package Description: 550 mL in 1 BOTTLE (54948-100-01)

NDC Information of BAEKNYONDONGAN TREATMENT

NDC Code 54948-100-01
Proprietary Name BAEKNYONDONGAN TREATMENT
Package Description 550 mL in 1 BOTTLE (54948-100-01)
Product NDC 54948-100
Product Type Name HUMAN OTC DRUG
Non Proprietary Name WITCH HAZEL
Dosage Form Name SOLUTION
Route Name TOPICAL
Start Marketing Date 20110803
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name MIX & MATCH CO., LTD.
Substance Name WITCH HAZEL
Strength Number .55
Strength Unit mL/550mL
Pharmaceutical Classes

Complete Information of BAEKNYONDONGAN TREATMENT


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