Class I · High risk
ClearLife Allergy 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 62795-4006-09 recalled?
Clearlife Extra Strength · 1 BOTTLE, PUMP in 1 CARTON (62795-4006-9) / 20 mL in 1 BOTTLE, PUMP
Yes — this exact package was recalled
1 FDA recall names the code 62795-4006-09 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
- ONION, GALPHIMIA GLAUCA FLOWERING TOP, HISTAMINE DIHYDROCHLORIDE, LUFFA OPERCULATA FRUIT, SULFUR, AMBROSIA ARTEMISIIFOLIA WHOLE, EUPHRASIA STRICTA and SCHOENOCAULON OFFICINALE SEED
- Strength
- ONION 4 [hp_X]/20mL; GALPHIMIA GLAUCA FLOWERING TOP 4…
- Form
- Spray · Nasal
- Labeler
- MediNatura Inc.
- Type
- Human OTC Drug
- Product code
- 62795-4006
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
- 62795-4005 ReBoost 1
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