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CERTAIN DRI ROLL-ON

NDC 69693-715, Aluminum Chloride, liquid, from Clarion Brands, LLC.

Product NDC
69693-715
Status
Listed
Labeler
Clarion Brands, LLC
Dosage form
LIQUID
Route
TOPICAL
Product type
HUMAN OTC DRUG
Marketing category
OTC MONOGRAPH DRUG
Application
M019
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/69693-715 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ALUMINUM CHLORIDE.12 mg/mL
Package NDCNDC-11Package
69693-715-01696930715011 APPLICATOR in 1 POUCH (69693-715-01) / 1.3 mL in 1 APPLICATOR
69693-715-12696930715121 BOTTLE, WITH APPLICATOR in 1 CARTON (69693-715-12) / 35.5 mL in 1 BOTTLE, WITH APPLICATOR
69693-715-20696930715201 BOTTLE, WITH APPLICATOR in 1 CARTON (69693-715-20) / 2 mL in 1 BOTTLE, WITH APPLICATOR

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 69693-715 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/69693-715 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 69693-715. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.