United States · FDA National Drug Code directory
Mentholatum Natural Ice Original
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
- 10742-3004_4dbf3ecb-629f-bbfc-e063-6294a90ad6a0
- Product NDC
- 10742-3004
- Form
- OINTMENT
- Composition / generic term
- dimethicone, octinoxate, octisalate
- Labeler
- The Mentholatum Company
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 19990119
- Source listing expiry
- 20271231
Source-listed ingredients
- OCTISALATE — 50 mg/g
- DIMETHICONE — 10 mg/g
- OCTINOXATE — 75 mg/g
These values do not establish equivalence or a dose recommendation.
Packages
- 1 TUBE in 1 BLISTER PACK (10742-3004-2) / 4.2 g in 1 TUBE · 10742-3004-2
- 1 TUBE in 1 BLISTER PACK (10742-3004-3) / 4.5 g in 1 TUBE · 10742-3004-3
- 4.5 g in 1 TUBE (10742-3004-4) · 10742-3004-4
- 4.2 g in 1 TUBE (10742-3004-8) · 10742-3004-8
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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