FDA.reportPublic FDA data

Tagrid Feminine Itch Relief Cream Antifungal Formula Clotrimazole 1%

Manufacturer
TAGRID LLC
Effective date
2026-05-15
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
daily-update
Hydrated at
2026-09-26 01:01:52

Label at a glance#

ProductTagrid Feminine Itch Relief Cream Antifungal Formula Clotrimazole 1%
Active ingredientCLOTRIMAZOLE
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient:

  1. Clotrimazole 1%

OTC - PURPOSE SECTION

  1. Antifungal

INDICATIONS & USAGE SECTION

Uses:

Temporarily relieves external vaginal itching, burning, and discomfort caused by yeast infections, and helps treat the associated irritation.

WARNINGS SECTION

For external use only.

OTC - DO NOT USE SECTION

Do not use:

  • Do not use On children under 2 years of age unless directed by a doctor.

OTC - WHEN USING SECTION

When using this product

  • Avoid contact with eyes. If contact occurs, rinse thoroughly with water. Keep out of reach of children.

OTC - STOP USE SECTION

Stop use and ask a doctor if

  • Irritation occurs.
  • There is no improvement within 4 weeks.
  • Discomfort persists.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

DOSAGE & ADMINISTRATION SECTION

Directions

  • Wash the affected area and dry thoroughly.
  • Apply a thin layer over the affected area twice daily (morning and night) or as directed by a doctor.
  • Supervise children in the use of this product.
  • If the condition persists, consult a doctor.

INACTIVE INGREDIENT SECTION

Ingredients:

  • Aqua
  • Glycerin
  • Tea Tree Oil
  • Olive Oil
  • Wormwood
  • Solidago Decurrens Fruiting Top
  • Gleditsia Sinensis Fruit
  • Aloe Vera Extract

OTC - QUESTIONS SECTION

Questions?

support@tagridLLC.com

OTHER SAFETY INFORMATION

Other Information

  • Store at 59-86°F (15-30°C).
  • Close the cap tightly after use.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

FEMININE ITCH RELIEF CREAM tagFEMININE ITCH RELIEF CREAM tag

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
Data codeCode 128X0052Q63X1FEMININE ITCH RELIEF CREAM.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
b64d2752-34ef-378a-1f4f-8bff32b0d1aeProduct name420250626
cb7783e0-feaa-7e56-fb3b-d43b6efa77c9Product name220250121
ebc62596-fc97-4d03-9483-7ba095d25db7Product name120151210
f31c883b-7ebf-1c60-f3b6-4ba41e8ff7a6Product name220151106
f5395dd2-4395-d8c6-3477-8c2d4a2f951cProduct name120140508

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
85384-002385384-0023-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
Water059QF0KO0RIACT
GlycerinPDC6A3C0OXIACT
Tea Tree OilVIF565UC2GIACT
Olive Oil6UYK2W1W1EIACT
WormwoodF84709P2XVIACT
Solidago Decurrens Fruiting Top6M6NP03LMKIACT
Gleditsia Sinensis FruitA6W0J6UO7QIACT
Aloe Vera LeafZY81Z83H0XIACT
CLOTRIMAZOLEG07GZ97H65ACTIB

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
22026-05-15weekly-update2026-07-17 21:43:29
12026-05-15full-release2026-06-01 01:57:37

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
544212f0-c045-479e-9dae-6248b324e144fe76e89c-470c-4903-bc8d-3fcdaee47d5a2026-05-15WarningsExact identifier
spl set id: fe76e89c-470c-4903-bc8d-3fcdaee47d5a

Reported adverse events (FAERS/openFDA)#

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