10742-3004 : Mentholatum Natural Ice Topical Ointment


NDC: 10742-3004
Labeler: The Mentholatum Company
Product Type: Human OTC Drug
Drug Name: Mentholatum Natural Ice Original
Dosage Form: Topical Ointment
Application #: part352
Rev. Date: 


NDC Package Codes:

  • 10742-3004-1: 1 TUBE IN 1 BLISTER PACK (10742‑3004‑1) > 4.5 G IN 1 TUBE
  • 10742-3004-2: 1 TUBE IN 1 BLISTER PACK (10742‑3004‑2) > 4.2 G IN 1 TUBE
  • 10742-3004-3: 1 TUBE IN 1 BLISTER PACK (10742‑3004‑3) > 4.5 G IN 1 TUBE
  • 10742-3004-4: 4.5 G IN 1 TUBE (10742‑3004‑4)
  • 10742-3004-5: 4.5 G IN 1 TUBE (10742‑3004‑5)
  • 10742-3004-8: 4.2 G IN 1 TUBE (10742‑3004‑8)
  • 10742-3004-9: 4.5 G IN 1 TUBE (10742‑3004‑9)

Active Ingredients:

  • Dimethicone
  • Octinoxate
  • Octisalate

Dosage Strength:

  • 10 mg/g
  • 75 mg/g
  • 50 mg/g

Pharmaceutical Classes:

  • Skin Barrier Activity [PE]

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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.