Quick answers
- What is Chlorhexidine gluconate and propylene glycol used for?
- The Drug Facts label of Neutraflush (Aero Healthcare) lists these uses: A preservative for use in potable self-contained emergency eyewash stations.
- Do I need a prescription for Chlorhexidine gluconate and propylene glycol?
- No. The products on this page are sold without a prescription (over the counter).
- Is a store brand the same as the name brand?
- Products listed together below have the same active ingredients, in the same amount and the same form, as registered with the FDA. Inactive ingredients (such as colors, flavors and fillers) and package sizes can differ. Compare the “Active ingredient” box on both packages, and ask a pharmacist if you are not sure.
- Has Chlorhexidine gluconate and propylene glycol been recalled?
- No recall linked to these products appears in the FDA enforcement reports we use.
Drug Facts label
Every over-the-counter medicine must carry a “Drug Facts” box in the same order, set by FDA rules. Below is the label of one product for each common strength and form, quoted word for word. Your own package can differ (for example, children’s products have other directions): always follow the label on your package.
Neutraflush · Aero Healthcare
Chlorhexidine gluconate 145.6 kg/2800 L · Propylene glycol 280 kg/2800 L, liquid (ophthalmic)
Active ingredient
Ingredients Chlorhexidine gluconate 1% w/v Purified Water, Propylene Glycol
Purpose
Preservative
Uses
A preservative for use in potable self-contained emergency eyewash stations
Warnings
For external use only. In case of contact with eye in undiluted form, flush with clean water
Do not use
in full strength
When using this product
do not change dilution or use with other chemicals do not reuse
Stop use and ask a doctor if
you have any of the following changes in vision eye pain condition worsens or persists continued redness or irritations of the eye
Keep out of reach of children
Keep out of reach of children
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
wear protective eyewear and gloves clean potable eyewash station and rinse with potable water partially fill station with potable water remove tamper evident seal and cap of bottle add entire contents of the bottle to the eyewash station container fill the station to the manufacturer's required level date and initial inspection tag station should be cleaned and refilled every 120 days when using this product in advance of emergency, add the concentrate to potable water to have solution available
Inactive ingredients
Purified Water
Questions?
Call (845) 618-7037 8 a.m. to 5 p.m. EST Mon-Fri
— FDA label of Neutraflush, Aero Healthcare, effective July 24, 2026. See the official label on DailyMed →
This page is not medical advice. Read the label on your package, and ask a pharmacist or doctor if you are not sure a medicine is right for you, for your child, or with your other medicines.
Same medicine, other brands
Each group lists the products that have exactly the same active ingredients, in the same amount and form, as registered with the FDA (NDC Directory). A store brand in the same group has the same medicine as the name brand; inactive ingredients, flavors and package sizes can differ. Each product links to its own official label.
Chlorhexidine gluconate 145.6 kg/2800 L · Propylene glycol 280 kg/2800 L · liquid (ophthalmic) · 4 products
Companies that sell this medicine
The company named on the package (maker or distributor), as listed in the FDA NDC Directory, with its number of over-the-counter products of this medicine.
- Aero Healthcare1 product
- Acme United Corporation1 product
- Global Equipment Company1 product
- Niagara Pharmaceuticals Inc.1 product
Recalls
No recall linked to these products (by their NDC code or label) appears in the FDA enforcement reports.
Next steps
- Find a pharmacy near youA pharmacist can answer questions about this label
- Latest FDA drug recallsPrescription and over-the-counter, newest first
- All over-the-counter medicinesSearch by ingredient, brand or Spanish name
Sources
- Drug labeling (SPL, openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026
- FDA rule for the Drug Facts label (21 CFR 201.66)
Only medicines marketed under FDA rules for nonprescription drugs (an FDA monograph or an FDA approval) are listed. Homeopathic products are not listed: the FDA does not evaluate them for safety or effectiveness.