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Diphenhydramine Hydrochloride and Zinc Acetate

NDC 51672-2089, Diphenhydramine Hydrochloride and Zinc Acetate, cream, from Sun Pharmaceutical Industries, Inc..

Product NDC
51672-2089
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
CREAM
Route
TOPICAL
Product type
HUMAN OTC DRUG
Marketing category
OTC MONOGRAPH DRUG
Application
M017
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51672-2089 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DIPHENHYDRAMINE HYDROCHLORIDE20 mg/g
  • ZINC ACETATE1 mg/g

Pharmacologic classes

Copper Absorption Inhibitor [EPC]; Decreased Copper Ion Absorption [PE]; Histamine H1 Receptor Antagonists [MoA]; Histamine-1 Receptor Antagonist [EPC]

Package NDCNDC-11Package
51672-2089-2516722089021 TUBE in 1 CARTON (51672-2089-2) / 28.4 g in 1 TUBE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

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

Use it

Look up 51672-2089 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51672-2089 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51672-2089. 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.