The Recall Desk
Agency classClass IIIOur severity:LowFDA (Drugs)·D-1268-2020·Announced 2020-05-20

ChapStick Total Hydration Moisture Tint Recalled for Packaging Separation

Glaxosmithkline is recalling ChapStick Total Hydration Moisture Tint Pretty in Pink due to observed separation in the secondary packaging.

The agency’s classification

FDA (Drugs): Class III

Class III is a situation in which use of or exposure to a violative product is not likely to cause adverse health consequences.

This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work

What this means for you

Our assessment, not the agency’s: severity 1/5 (Low).

Cosmetic or documentation issue. No expected health impact, but the manufacturer is correcting the affected products.

Our severity reasoning: The recall is classified as FDA Class III, which by definition is unlikely to cause adverse health consequences, and the issue is limited to packaging separation.

Plain-English summary

Glaxosmithkline Consumer Healthcare Holdings is recalling 360 packages of ChapStick Total Hydration Moisture Tint Pretty in Pink (Zinc Oxide). The product is marketed by Pfizer and is available nationwide. The recall involves specific lot numbers 9343AA and 9343BA.

The recall was initiated because of observed separation in the secondary packaging, specifically between the blister and the backer card. This is a Class III recall, indicating that the product is not likely to cause adverse health consequences.

Consumers who have this product should stop using it and contact the recalling firm for further instructions or a refund. The product is an over-the-counter topical drug containing zinc oxide.

The recalled product

Product
CHAPSTICK TOTAL HYDRATION MOISTURE TINT PRETTY IN PINK (ZINC OXIDE)
Brand
CHAPSTICK TOTAL HYDRATION MOISTURE TINT PRETTY IN PINK
Manufacturer
Glaxosmithkline Consumer Healthcare Holdings
Category
Drug — OTC Topical
Hazard
Affected units
360

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (2)

  • Lot #: 9343AA
  • 9343BA

Distribution

Distributed nationwide across the United States.

Part of a larger recall action

This product is one of 3 recalled by Glaxosmithkline Consumer Healthcare Holdings under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 3 products in this recall →

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