CLASS III Drug recall · Reported 20 May 2020 · FDA Enforcement Report
ChapStick Total Hydration Moisture + Tint + SPF15 Peachy Keen recalled
Glaxosmithkline Consumer Healthcare Holdings is recalling ChapStick Total Hydration Moisture + Tint + SPF15 Peachy Keen, distributed nationwide in the US. The recall was initiated on 20 Apr 2020 and the FDA has classified it as Class III.
Check your package
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
Recall details
- Recall number
- D-1266-2020
- FDA event ID
- 85500
- Recalling firm
- Glaxosmithkline Consumer Healthcare Holdings, Warren, NJ
- Manufacturer
- Haleon US Holdings LLC
- Classification
- Class III
- Status
- Terminated
- Recall initiated
- 20 Apr 2020
- FDA classified
- 13 May 2020
- Reported
- 20 May 2020
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Packaging Defects
- Drug class
- Sunscreen & Personal Care
Timeline
| 20 Apr 2020 | Recall initiated by company | |
| 13 May 2020 | Classified by FDA | +23 days |
| 20 May 2020 | Published in enforcement report | +7 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Labeling: Not elsewhere classified: Observed separation in the secondary packaging in the blister and the backer card
Packaging recalls include wrong labels, wrong products in the wrong bottle, missing leaflets, short-filled or empty capsules and seals that fail.
Product as listed by the FDA
ChapStick Total Hydration Moisture + Tint + SPF15 Peachy Keen Net Wt. 0.08 OZ (2.2g) Marketed by: Pfizer, Madison, NJ 07940 USA, NDC 0573-0871-08
Where it was distributed
Nationwide
Questions about this recall
Why was it recalled?
Labeling: Not elsewhere classified: Observed separation in the secondary packaging in the blister and the backer card
Which lots are affected?
Lot #: 9344AA, 9345AA
Where was it sold?
Nationwide
What should I do if I have it?
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
What does Class III mean?
Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
Other products in this recall event
2 other products · FDA event 85500This product is part of a recall event; the main page for the event is ChapStick Total Hydration Moisture + Tint + SPF15 Very Berry recalled.
| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| CLASS III | ChapStick Total Hydration Moisture + Tint + SPF15 Very Berry recalledChapstick Total Hydration Moisture Tint Very Berry | Glaxosmithkline Consumer Healthcare Holdings | Packaging Defects | Nationwide | |
| CLASS III | ChapStick Total Hydration Moisture + Tint + SPF15 Pretty in Pink recalledChapstick Total Hydration Moisture Tint Pretty In Pink | Glaxosmithkline Consumer Healthcare Holdings | Packaging Defects | Nationwide |
More recalls from Glaxosmithkline Consumer Healthcare Holdings
All 26| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | TUMS Antacid, Calcium Carbonate USP 1000 mg recalled | GlaxoSmithKline Consumer Healthcare Holdings | Foreign Material | Nationwide |
| Drug | CLASS II | TUMS Antacid, Calcium Carbonate USP 1000 mg recalled | GlaxoSmithKline Consumer Healthcare Holdings | Foreign Material | Nationwide |
| Drug | CLASS II | TUMS Antacid, Calcium Carbonate USP 1000 mg recalledTums | GlaxoSmithKline Consumer Healthcare Holdings | Foreign Material | Nationwide |
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All 12| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | WeCare, Zinc Oxide Ointment recalled by Blossom PharmaceuticalsZinc Oxide | Blossom Pharmaceuticals | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Nivagen, Zinc Oxide Ointment recalled by Blossom PharmaceuticalsNivagen Zinc Oxide | Blossom Pharmaceuticals | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Nivagen, Zinc Oxide Ointment USP, Zinc Oxide 20 % recalledNivagen Zinc Oxide | Blossom Pharmaceuticals | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Dynashield cream recalled by Blossom PharmaceuticalsDynashield | Blossom Pharmaceuticals | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Dynashield Skin Protectant recalled by Blossom PharmaceuticalsDynashield | Blossom Pharmaceuticals | Manufacturing (CGMP) Deviations | Nationwide |