60512-0002 : Eczema Relief Oral Pellet


NDC60512-0002
Labeler: Homeolab USA Inc.
Product Type: Human OTC Drug
Drug Name: Eczema Relief
Dosage Form: Oral Pellet
Rev. Date: 


NDC Package Codes:

  • 60512-0002-1: 80 PELLET IN 1 TUBE (60512‑0002‑1)

Active Ingredients:

  • Aluminum Oxide
  • Amanita Muscaria Whole
  • Kerosene
  • Potassium Arsenite Anhydrous
  • Sepia Officinalis Juice
  • Sodium Chloride

Dosage Strength:

  • 6 [hp_C]/1
  • 6 [hp_C]/1
  • 6 [hp_C]/1
  • 6 [hp_C]/1
  • 6 [hp_C]/1
  • 6 [hp_C]/1

Related Products:

Based on records with the same trade name.
  • 0363-1289 Eczema Relief 10 mg/11g Topical Ointment by Walgreens
  • 55910-653 Eczema Relief 10 mg/11g Topical Ointment by Old East Main Co
  • 61727-326 Eczema Relief Sublingual Pellet by Homeocare Laboratories
  • 66096-192 Eczema Relief Oral Liquid by Ohm Pharma Inc.
  • 71976-301 Eczema Relief Topical Ointment by Littles Skin Care, Inc
  • 80551-301 Eczema Relief 1 g/100g Topical Cream by Acutens, Inc.
  • 82960-256 Eczema Relief 1 g/100ml Topical Cream by Rosemont Ventures, Inc.

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.