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NDC 10742-3051, dimethicone, octinoxate, octisalate, oxybenzone, ointment, from The Mentholatum Company.

Product NDC
10742-3051
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/10742-3051 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DIMETHICONE20 mg/g
  • OCTINOXATE75 mg/g
  • OCTISALATE30 mg/g
  • OXYBENZONE30 mg/g

Pharmacologic classes

Skin Barrier Activity [PE]

Package NDCNDC-11Package
10742-3051-1107423051011 TUBE in 1 BLISTER PACK (10742-3051-1) / 2 g in 1 TUBE
10742-3051-2107423051022 g in 1 TUBE (10742-3051-2)
10742-3051-3107423051033 TUBE in 1 BLISTER PACK (10742-3051-3) / 2 g in 1 TUBE
10742-3051-9107423051092 TUBE in 1 BLISTER PACK (10742-3051-9) / 2 g in 1 TUBE

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 10742-3051 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/10742-3051 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 10742-3051. 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.