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Pro Numb Sensitive Skin

NDC 83389-112, Numbing Spray, spray, from Pro Numb Tattoo Numbing Spray LLC.

Product NDC
83389-112
Status
Listed
Labeler
Pro Numb Tattoo Numbing Spray LLC
Dosage form
SPRAY
Route
TOPICAL
Product type
HUMAN OTC DRUG
Marketing category
UNAPPROVED DRUG OTHER
Application
—
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/83389-112 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • EPINEPHRINE HYDROCHLORIDE.1 mg/100mL
  • LIDOCAINE HYDROCHLORIDE4.2 mg/100mL

Pharmacologic classes

Adrenergic alpha-Agonists [MoA]; Adrenergic beta-Agonists [MoA]; Amide Local Anesthetic [EPC]; Amides [CS]; Antiarrhythmic [EPC]; Catecholamine [EPC]; Catecholamines [CS]; Local Anesthesia [PE]; alpha-Adrenergic Agonist [EPC]; beta-Adrenergic Agonist [EPC]

Package NDCNDC-11Package
83389-112-1183389011211120 mL in 1 BOTTLE, SPRAY (83389-112-11)

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 83389-112 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/83389-112 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 83389-112. 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.