Class I · High risk
ReBoost Nasal Spray
Microbial Contamination of Non-Sterile Products: The products have been found to contain yeast/mold and microbial contamination identified as Achromobacter.
National Drug Code
Is NDC 62795-4005-09 recalled?
ReBoost · 1 BOTTLE, PUMP in 1 CARTON (62795-4005-9) / 20 mL in 1 BOTTLE, PUMP
Yes — this exact package was recalled
1 FDA recall names the code 62795-4005-09 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.
1 of these recalls is still ongoing.
- Active ingredient
- SILVER NITRATE,EUPHORBIA RESINIFERA RESIN, CALCIUM SULFIDE, GOLDENSEAL, POTASSIUM DICHROMATE,LUFFA OPERCULATA FRUIT, SODIUM CARBONATE, ECHINACEA UNSPECIFIED, CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE and PULSATILLA VULGARIS
- Strength
- SILVER NITRATE 10 [hp_X]/20mL; EUPHORBIA RESINIFERA RESIN 4…
- Form
- Spray · Nasal
- Labeler
- MediNatura
- Type
- Human OTC Drug
- Product code
- 62795-4005
Recalls naming this package
Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.
Other recalled products from this labeler
- 62795-4006 Clearlife Extra Strength 1
Free recall alerts
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