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NDC 67172-999, Glycerin and Naphazoline Hydrochloride and Zinc Sulfate, liquid, from Prestige Brands Holdings, Inc..

Product NDC
67172-999
Status
Listed
Labeler
Prestige Brands Holdings, Inc.
Dosage form
LIQUID
Route
OPHTHALMIC
Product type
HUMAN OTC DRUG
Marketing category
OTC MONOGRAPH DRUG
Application
M018
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/67172-999 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • GLYCERIN2.5 mg/mL
  • NAPHAZOLINE HYDROCHLORIDE.12 mg/mL
  • ZINC SULFATE2.5 mg/mL

Pharmacologic classes

Allergens [CS]; Cell-mediated Immunity [PE]; Copper Absorption Inhibitor [EPC]; Decreased Copper Ion Absorption [PE]; Glycerol [CS]; Increased Histamine Release [PE]; Increased IgG Production [PE]; Non-Standardized Chemical Allergen [EPC]

Package NDCNDC-11Package
67172-999-01671720999011 BOTTLE, DROPPER in 1 BOX (67172-999-01) / 15 mL in 1 BOTTLE, DROPPER

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 67172-999 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/67172-999 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.