United States · FDA National Drug Code directory
Aquaphor Itch Relief
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
- 10356-120_4615f353-0a2d-5ff1-e063-6394a90a77e3
- Product NDC
- 10356-120
- Form
- OINTMENT
- Composition / generic term
- Hydrocortisone
- Labeler
- Beiersdorf Inc
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20201101
- Source listing expiry
- 20261231
Source-listed ingredients
- HYDROCORTISONE — 1 g/100g
These values do not establish equivalence or a dose recommendation.
Packages
- 28 g in 1 TUBE (10356-120-04) · 10356-120-04
- 56 g in 1 TUBE (10356-120-07) · 10356-120-07
- .9 g in 1 PACKET (10356-120-30) · 10356-120-30
- 1 TUBE in 1 CARTON (10356-120-52) / 28 g in 1 TUBE (10356-120-04) · 10356-120-52
- 2 TUBE in 1 CARTON (10356-120-53) / 28 g in 1 TUBE (10356-120-04) · 10356-120-53
- 1 TUBE in 1 CARTON (10356-120-54) / 56 g in 1 TUBE (10356-120-07) · 10356-120-54
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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