Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
RxRecalls Get alerts

National Drug Code

Is NDC 69949-0153-01 recalled?

Impeccable Skin - Sand · 56.7 g in 1 TUBE (69949-153-01)

Yes — this exact package was recalled

1 FDA recall names the code 69949-0153-01 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
Zinc Oxide
Strength
ZINC OXIDE 150 mg/g
Form
Cream · Topical
Labeler
Synchronicity Spa, Inc. DBA Suntegrity
Type
Human OTC Drug
Product code
69949-0153

Recalls naming this package

Class II · Moderate risk

suntegrity

CGMP Deviations

Ongoing cGMP deviation Synchronicity Spa INC, Dba Sunte D-0589-2024

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