United States · FDA National Drug Code directory
Durashield
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 85131-013_b9f737e2-25dc-44cc-aa07-a5a77758473c
- Product NDC
- 85131-013
- Form
- LOTION
- Composition / generic term
- benzalkonium chloride
- Labeler
- Advanced Biomedical Incorporated
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20241218
- Source listing expiry
- 20261231
Source-listed ingredients
- BENZALKONIUM CHLORIDE — .13 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- .33 mL in 1 BOTTLE (85131-013-00) · 85131-013-00
- 60 mL in 1 BOTTLE (85131-013-02) · 85131-013-02
- 118 mL in 1 BOTTLE (85131-013-04) · 85131-013-04
- 237 mL in 1 BOTTLE, PUMP (85131-013-08) · 85131-013-08
- 355 mL in 1 BOTTLE, PUMP (85131-013-12) · 85131-013-12
- 473 mL in 1 BOTTLE, PUMP (85131-013-16) · 85131-013-16
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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