FDA.reportPublic FDA data

Thera Care

Manufacturer
Jiangsu Intco Medical Products Co Ltd
Effective date
2020-04-21
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:34:39

Label at a glance#

ProductThera Care
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Wet hands thoroughly with product and allow to dry without wiping For children under 6, use only under adult supervision Not recommended for infants

Storage and handling

Store at 68-77℉(20-25℃) May discolor some fabrics Harmful to wood finishes and plastics

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 70% v/v. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

To help decrease bacteria on the skin. Recommended for repeat use.

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from heat or flame

Do not use

OTC - DO NOT USE SECTION

  • Around eyes
  • In ears and mouth

OTC - WHEN USING SECTION

  • Keep out of eyes. In case of contact, rinse eyes thoroughly with water
  • Avoid Contact with broken skin
  • Do not inhale or ingest

OTC - STOP USE SECTION

If irritation or redness develops

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away, 800-222-1222.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Wet hands thoroughly with product and allow to dry without wiping
  • For children under 6, use only under adult supervision
  • Not recommended for infants

Other information

STORAGE AND HANDLING SECTION

  • Store at 68-77℉(20-25℃)
  • May discolor some fabrics
  • Harmful to wood finishes and plastics

Inactive ingredients

INACTIVE INGREDIENT SECTION

aloe barbadensis extract, carbomer, lemon oil, glycerin, Triethanolamine, water

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Thera-Care-Final-74201-267-01-NDCThera-Care-Final-74201-267-01-NDC236 mL NDC: 74201-267-01236 mL NDC: 74201-267-01

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
74201-267-012024-07-21C16284748780-11030e365-23e1-111a-e063-dadaa90a10e2a3cdabb7-80c5-a386-e053-2a95a90ab1c1
74201-267-012024-01-30C16284748780-11030e365-23e1-111a-e063-dadaa90a10e2a3cdabb7-80c5-a386-e053-2a95a90ab1c1

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74201-26774201-267-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
LEMON OILI9GRO824LLIACT
TROLAMINE9O3K93S3TKIACT
ALOE VERA LEAFZY81Z83H0XIACT
GLYCERINPDC6A3C0OXIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB

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
1dc0132f-3542-f100-e063-6394a90ac82ba3cdabb7-80c5-a386-e053-2a95a90ab1c12024-07-21WarningsExact identifier
spl set id: a3cdabb7-80c5-a386-e053-2a95a90ab1c1

Reported adverse events (FAERS/openFDA)#

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