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Mentholatum Natural Ice Original

NDC 10742-3004, dimethicone, octinoxate, octisalate, ointment, from The Mentholatum Company.

Product NDC
10742-3004
Status
Listed
Labeler
The Mentholatum Company
Dosage form
OINTMENT
Route
TOPICAL
Product type
HUMAN OTC DRUG
Marketing category
OTC MONOGRAPH DRUG
Application
M020
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/10742-3004 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • OCTISALATE50 mg/g
  • DIMETHICONE10 mg/g
  • OCTINOXATE75 mg/g

Pharmacologic classes

Skin Barrier Activity [PE]

Package NDCNDC-11Package
10742-3004-2107423004021 TUBE in 1 BLISTER PACK (10742-3004-2) / 4.2 g in 1 TUBE
10742-3004-3107423004031 TUBE in 1 BLISTER PACK (10742-3004-3) / 4.5 g in 1 TUBE
10742-3004-4107423004044.5 g in 1 TUBE (10742-3004-4)
10742-3004-8107423004084.2 g in 1 TUBE (10742-3004-8)

Linked data

RxNorm, label and prices

RxNorm concepts

RxNorm links no concept to this product's packages.

Related lookups

No FDA label, Medicare Part B payment limit or NADAC price is linked to this product.

Use it

Look up 10742-3004 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/10742-3004 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 10742-3004. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.