62011-0196 : Dry Eye Relief Ophthalmic Liquid


NDC62011-0196
Labeler: Mckesson Corporation
Product Type: Human OTC Drug
Drug Name: Dry Eye Relief
Dosage Form: Ophthalmic Liquid
Application #: part349
Rev. Date: 


NDC Package Codes:

  • 62011-0196-1: 1 BOTTLE, PLASTIC IN 1 CARTON (62011‑0196‑1) > 15 ML IN 1 BOTTLE, PLASTIC

Active Ingredients:

  • Hypromelloses
  • Glycerin
  • Polyethylene Glycol 400

Dosage Strength:

  • .2 g/100mL
  • .2 g/100mL
  • 1 g/100mL

Pharmaceutical Classes:

  • Allergens [CS]
  • Cell-mediated Immunity [PE]
  • Glycerol [CS]
  • Increased Histamine Release [PE]
  • Increased IgG Production [PE]
  • Non-Standardized Chemical Allergen [EPC]

Related Products:

Based on records with the same trade name.
  • 49348-095 Dry Eye Relief Ophthalmic Liquid by Mckesson Corporation
  • 53799-300 Dry Eye Relief Ophthalmic Solution/ Drops by Similasan Ag
  • 53799-375 Dry Eye Relief Ophthalmic Solution/ Drops by Similasan Ag
  • 59262-345 Dry Eye Relief Ophthalmic Solution/ Drops by Similasan Corporation
  • 59262-351 Dry Eye Relief Ophthalmic Solution/ Drops by Similasan Corporation
  • 59262-352 Dry Eye Relief Ophthalmic Solution/ Drops by Similasan Corporation
  • 59262-374 Dry Eye Relief Ophthalmic Solution/ Drops by Similasan Corporation
  • 59262-375 Dry Eye Relief Ophthalmic Solution/ Drops by Similasan Corporation
  • 70000-0088 Dry Eye Relief Ophthalmic Gel by Cardinal Health
  • 70000-0089 Dry Eye Relief 10 mg/ml Ophthalmic Gel by Cardinal Health

NDC QR Code

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NDC 62011-0196 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.