HEB Medicated Cornstarch Body Powder

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: HEB Medicated Cornstarch Body Powder
Generic name: MENTHOL
Manufacturer: Davion, Inc
Product type: HUMAN OTC DRUG
SPL set ID: df1331fb-48df-4f21-8564-0468078fd12d
SPL ID: d07cb2d2-d35b-4fb8-b467-b6243e4299fc
Version: 4
Effective date: 2025-12-29
Source export date: 2026-09-28
Source partition: 11
Source file: https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:17:10

Harmonized routes table
Harmonized routes
TOPICAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 11 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		HEB Medicated Cornstarch Body Powder	openfda.brand_name
generic name		MENTHOL	openfda.generic_name
manufacturer name		Davion, Inc	openfda.manufacturer_name
ndc	package	42669-217-10	openfda.package_ndc
ndc	product	42669-217	openfda.product_ndc
ndc11	package	42669021710	derived:openfda.package_ndc
rxcui		1431703	openfda.rxcui
spl id		d07cb2d2-d35b-4fb8-b467-b6243e4299fc	id
spl set id		df1331fb-48df-4f21-8564-0468078fd12d	set_id
unii		L7T10EIP3A	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warning For external use only Avoid contact with eyes Stop use and ask a doctor if condition worsens symptoms persist for more than 7 days or clear up and occur again within few days Keep out of reach of children In case of accidental ingestion, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.