# FDA recall D-905-2013

> **Novartis Consumer Health** · Class III · drug recall initiated 2013-08-06.

## Product

Maalox Advanced Maximum Strength Antacid & Antigas (calcium carbonate and simethicone) chewable tablets, 1000 mg/60 mg, Assorted Fruit flavor, packaged in a) 35-count (NDC 0067-6279-35) (UPC 3 0067-0343-35 4); b) 65-count (NDC 0067-6279-65) (UPC 3 0067-0343-65 1); and c) 90-count (NDC 0067-6279-90) (UPC 3 0067-0343-90 3) tablets per bottle, Distributed by: Novartis Consumer Health, Inc., Parsippany, NJ  07054-0622.

## Reason for recall

Labeling: Incorrect Or Missing Lot and/or Exp Date: The lot number and/or expiration date may be illegible on the outer plastic bottle packaging.

## Distribution

Nationwide, Canada, and Panama.

## Key facts

- **Recall number:** D-905-2013
- **Recalling firm:** Novartis Consumer Health
- **Classification:** Class III
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2013-08-06
- **Report date:** 2013-08-28
- **Termination date:** 2014-11-04

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Lincoln, NE, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-905-2013

## Citation

> AI Analytics. FDA recall D-905-2013. Retrieved 2026-05-25 from https://api.ai-analytics.org/recall/D-905-2013. Source: US FDA. Licensed CC0.

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