51672-1327 : Lustra-af 40 mg/g Topical Cream


NDC: 51672-1327
Labeler: Taro Pharmaceuticals U.S.a., Inc.
Product Type: Human Prescription Drug
Drug Name:  Lustra-af
Dosage Form: Topical Cream
Rev. Date: 


NDC Package Codes:

  • 51672-1327-3: 1 TUBE IN 1 CARTON (51672‑1327‑3) > 56.8 G IN 1 TUBE

Active Ingredients:

  • Hydroquinone

Dosage Strength:

  • 40 mg/g

Pharmaceutical Classes:

  • Melanin Synthesis Inhibitor [EPC]
  • Melanin Synthesis Inhibitors [MoA]
  • Depigmenting Activity [PE]

NDC QR Code

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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.