Why it was recalled
cGMP Deviations
Product description
Neutrogena Invisible Daily defense body spray sunscreen BROAD SPECTRUM SPF 60+, Avobenzone (3%), Homosalate (10%), Octisalate (5%), Octocrylene (10%), NET WT. 5.0 OZ. (141 g) aerosol can, Distributed by: JOHNSON & JOHNSON CONSUMER, INC. Skillman, NJ 08858, UPC 0 86800 11154 2
Lot numbers, UPCs & expiration codes
All lots within expiry.
Where it was sold
Nationwide in US
What to do if you have this product
- Compare the lot number and expiration date on your package with the codes above.
- Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
- If you have symptoms you think are related, contact your doctor. In an emergency call 911.
- Report side effects to FDA MedWatch at 1-800-FDA-1088.
Recall details
- Recall number
- D-0843-2021
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- Jul 14, 2021
- FDA report date
- Oct 6, 2021
- Quantity
- 88,380 cans
- Recall type
- Voluntary: Firm initiated
- Recalling firm
- Johnson & Johnson Consumer, Inc.
Original FDA data
Every field from FDA enforcement report D-0843-2021, exactly as published.
Show all FDA fields
- City
- Skillman
- State
- NJ
- Status
- Ongoing
- Country
- United States
- Event ID
- 88288
- Address
- 199 Grandview Rd
- Code information
- All lots within expiry.
- Postal code
- 08558-1311
- Report date
- Oct 6, 2021
- Product type
- Drugs
- Recall number
- D-0843-2021
- Classification
- Class II
- Recalling firm
- Johnson & Johnson Consumer, Inc.
- Product quantity
- 88,380 cans
- Reason for recall
- cGMP Deviations
- Voluntary / mandated
- Voluntary: Firm initiated
- Product description
- Neutrogena Invisible Daily defense body spray sunscreen BROAD SPECTRUM SPF 60+, Avobenzone (3%), Homosalate (10%), Octisalate (5%), Octocrylene (10%), NET WT. 5.0 OZ. (141 g) aerosol can, Distributed by: JOHNSON & JOHNSON CONSUMER, INC. Skillman, NJ 08858, UPC 0 86800 11154 2
- Distribution pattern
- Nationwide in US
- Recall initiation date
- Jul 14, 2021
- Initial firm notification
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Center classification date
- Sep 24, 2021