FDA.reportPublic FDA data

AA Top Medicated

Manufacturer
Albert Max, Inc.
Effective date
2018-01-12
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
legacy-cache
Hydrated at
2026-08-02 01:03:48

Label at a glance#

ProductAA Top Medicated
Active ingredientMENTHOL, METHYL SALICYLATE
Label structure8 sections

Indications and uses

Temporarily relieves minor aches and pains of muscles and joints due to: simple backache arthritis strains bruises sprains

Dosage and administration

adults and children 12 years of age and older: apply 3 to 4 drops of medicated oil to the affected area 1 or 2 times daily. After applying the product, a warm pad may be placed on the affected area for 10 minutes and then massage as shown in the illustrations. children under 12 years of age: consult your physician. refer to the above warnings; use otherwise than directed may be dangerous.

Storage and handling

store at 16° to 30°C (61° to 86°F) store in an airtight container

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Menthol 10%

Methyl Salicylate 5%

Purpose

OTC - PURPOSE SECTION

External analgesic

Uses

INDICATIONS & USAGE SECTION

Temporarily relieves minor aches and pains of muscles and joints due to:

  • simple backache
  • arthritis
  • strains
  • bruises
  • sprains

Warnings

WARNINGS SECTION

For external Use Only

Do not use

OTC - DO NOT USE SECTION

  • on wounds
  • on irritated or damaged skin
  • otherwise than as directed

When using this product

OTC - WHEN USING SECTION

  • avoid contact with the eyes or mucous membranes
  • do not bandage tightly

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • condition worsens
  • symptoms persist for more than 7 days
  • symptoms clear up and occur again within a few days
  • excessive irritation of the skin develops
  • nausea, vomiting, abdominal discomfort, diarrhea, or skin rash occurs

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • adults and children 12 years of age and older: apply 3 to 4 drops of medicated oil to the affected area 1 or 2 times daily. After applying the product, a warm pad may be placed on the affected area for 10 minutes and then massage as shown in the illustrations.
  • children under 12 years of age: consult your physician.
  • refer to the above warnings; use otherwise than directed may be dangerous.

Other information

STORAGE AND HANDLING SECTION

  • store at 16° to 30°C (61° to 86°F)
  • store in an airtight container

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Saposhnikoviae Radix, Artemisia Argyi Leaf, Moutan Cortex, Carpesii Fructus, Cimicifugae Rhizoma, Sophorae Flavescentis Radix, Impatiens Balsamina, Paeoniae Rubra Radix, Zanthoxyli Pericarpium, Glycyrrhizae Radix Et Rhizoma, Ocimum Basilicum, Notoginseng Radix Et Rhizoma, Carthami Flos, Ethyl Alcohol

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

A&A Top Medicated Oil

external analgesic

1.75FL OZ. (50mL)

Distributed By:

A&A Medical Supplies, Inc.

S. El Monte, CA 91733 USA

Made in Taiwan

PDPPDP

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
68233-810-012023-10-10C16284748780-1d6a99b39-e9e9-a426-e053-dadaa90af4c2A&A Top Medicated Oil
68233-810-012022-01-28C16284748780-1d6a99b39-e9e9-a426-e053-dadaa90af4c2A&A Top Medicated Oil

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 19 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
68233-81068233-810-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 16 matching rows.

Name, UNII, Kind table
NameUNIIKind
IMPATIENS BALSAMINA WHOLEZMK32KX641IACT
LICORICE61ZBX54883IACT
MENTHOLL7T10EIP3AACTIB
METHYL SALICYLATELAV5U5022YACTIB
OCIMUM BASILICUM WHOLEP4815JL4O3IACT
SAFFLOWER4VBL71TY4YIACT
SAPOSHNIKOVIA DIVARICATA WHOLELA61LWB4JHIACT
PAEONIA X SUFFRUTICOSA ROOT BARKBUG255FE7XIACT
ACTAEA CIMICIFUGA ROOT65J267BAZTIACT
SOPHORA FLAVESCENS ROOTIYR6K8KQ5KIACT
ZANTHOXYLUM PIPERITUM FRUIT PULP7PFC2VA251IACT
PANAX NOTOGINSENG ROOTGQX1C1175UIACT
PAEONIA LACTIFLORA WHOLEN44H57P7WGIACT
ALCOHOL3K9958V90MIACT
ARTEMISIA ARGYI LEAF2JYC99Q0WZIACT
CARPESIUM ABROTANOIDES FRUIT20C78R73NHIACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
074c03eb-4f98-1d0c-e063-6394a90a3aaa6193cc31-ab84-3240-e053-2991aa0a6ffb2023-10-09WarningsExact identifier
spl set id: 6193cc31-ab84-3240-e053-2991aa0a6ffb

Reported adverse events (FAERS/openFDA)#

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