Label: OPTIMEL MANUKA FORTE EYE GEL- glycerin gel
- NDC Code(s): 73024-429-10
- Packager: Melcare Biomedical Pty Ltd
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated April 4, 2023
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredients
- Purpose
- Uses
- Warnings
- Do not use
- When using this product
-
Stop use and ask a doctor if
- you experience eye pain changes in vision
- continued redness or irritation of the eye.
- condition worsens or persists for more than 72 hours.
- you have any reaction other than transient stinging and redness.
- You experience eye pain, change in vision, continued redness or irritation of the eye.
- Condition worsens
- Keep out of reach of children.
- Directions
- Other information
- Inactive ingredients
- Questions?
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
OPTIMEL MANUKA FORTE EYE GEL
glycerin gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73024-429 Route of Administration OPHTHALMIC Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN 2 mg in 1 mL Inactive Ingredients Ingredient Name Strength HONEY (UNII: Y9H1V576FH) WATER (UNII: 059QF0KO0R) ACACIA (UNII: 5C5403N26O) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73024-429-10 1 in 1 CARTON 07/19/2019 1 10 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part349 07/19/2019 Labeler - Melcare Biomedical Pty Ltd (743166886)