Mitchum Advance Control

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: Mitchum Advance Control
Generic name: ALUMINUM CHLOROHYDRATE
Manufacturer: Revlon Consumer Products Corp
Product type: HUMAN OTC DRUG
SPL set ID: 40b9968a-9025-5ed9-e054-00144ff88e88
SPL ID: 43158fa6-9a5d-1c85-e054-00144ff88e88
Version: 2
Effective date: 2016-12-07
Source export date: 2026-10-27
Source partition: 8
Source file: https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-27/2eee27992d1f29d82f827fd5be42f1314ed39ce4c497af5d81435ac6656a0957/drug-label-0008-of-0014.json.zip
Source manifest SHA-256: 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run: 20261027T193451Z
Imported at: 2026-10-27 20:23:19

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 · 25 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		part350	openfda.application_number
brand name		Mitchum Advance Control Sport	openfda.brand_name
brand name		Mitchum Advance Control Pure Fresh	openfda.brand_name
brand name		Mitchum Advance Control	openfda.brand_name
brand name		Mitchum Advance Control Powder Fresh	openfda.brand_name
generic name		ALUMINUM CHLOROHYDRATE	openfda.generic_name
manufacturer name		Revlon Consumer Products Corp	openfda.manufacturer_name
ndc	package	10967-636-04	openfda.package_ndc
ndc	package	10967-635-04	openfda.package_ndc
ndc	package	10967-637-04	openfda.package_ndc
ndc	package	10967-638-04	openfda.package_ndc
ndc	package	10967-649-04	openfda.package_ndc
ndc	product	10967-638	openfda.product_ndc
ndc	product	10967-649	openfda.product_ndc
ndc	product	10967-635	openfda.product_ndc
ndc	product	10967-636	openfda.product_ndc
ndc	product	10967-637	openfda.product_ndc
ndc11	package	10967063604	derived:openfda.package_ndc
ndc11	package	10967063504	derived:openfda.package_ndc
ndc11	package	10967064904	derived:openfda.package_ndc
ndc11	package	10967063704	derived:openfda.package_ndc
ndc11	package	10967063804	derived:openfda.package_ndc
spl id		43158fa6-9a5d-1c85-e054-00144ff88e88	id
spl set id		40b9968a-9025-5ed9-e054-00144ff88e88	set_id
unii		HPN8MZW13M	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

Warnings: Do not use on broken skin Stop Use if rash or irritation occurs. When using this product, keep away from face and mouth to avoid breathing in. Avoid spraying in eyes Contents under pressure Do not place in hot water or near radiators, stoves, or other sources of heat. Do not puncture or incinerate container or store at temperatures over 50C Flammable Do not use in presence of flame or spark. Keep out of reach of children

Reported adverse events (FAERS/openFDA)#

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