UNDA HAIR MOISTURIZING

Manufacturer
UNDA
Effective date
2016-07-24
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:46:36

Label at a glance#

ProductUNDA HAIR MOISTURIZING
Active ingredientEUCALYPTUS GLOBULUS LEAF, BAMBUSA VULGARIS TOP, SHEA BUTTER
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Bambusa Vulgaris Extract, Butyrospermum Parkii (Shea) Butter, Eucalyptus Globulus Leaf Oil

INACTIVE INGREDIENT SECTION

Cyclomethicone, Dipropylene Glycol, Cetearyl Alcohol, Cetearyl Glucoside, Caprylyl Glycol, Hydrolyzed Silk, Sciadopitys Verticillata Root Extract, Krameria Triandra Root Extract, Carbomer, Glyceryl Stearat, Glyceryl Stearate SE, Arginine, Decylene Glycol. Ethylhexylglycerin, Hexylene Glycol, Butylene Glycol, Totarol, Tocopheryl Acetate, Retinyl Palmitate, Allantoin, Phenylalanine, Proline, Threonine, Tryptophan, Valine, Pyridoxine, Ascorbic Acid, Polyquaternium-10, Dimethiconol

OTC - PURPOSE SECTION

Helps alleviate the concerns such as hair loss, dandruff, and dryness.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of the children


INDICATIONS & USAGE SECTION

  1. Wet your hair with plenty of lukewarm water.
  2. Use two pumps of Unda moisturizing shampoo (depending on hair length and amount of hair, three pumps may be applicable)
  3. Use your fingertips to rub your scalp and make plenty of bubbles.
  4. Enjoy its natural scent and massage lightly for 2~3minutes.
  5. Wash off with lukewarm water.
  6. Dry with dry towel.
  7. Use one pump of Unda moisturizing cream to apply directly on your hair thoroughly.
  8. Hair Dry

WARNINGS SECTION

1. Do not use in the following cases(Eczema and scalp wounds)

2.Side Effects

1)Due to the use of this product if rash, irritation, itching and symptopms of hypersnesitivity occur, dicontinue use and consult your phamacisr or doctor

3.General Precautions

1)If in contact with the eyes, wash out thoroughty with water If the symptoms are servere, seek medical advice immediately

2)This product is for exeternal use only. Do not use for internal use

4.Storage and handling precautions

1)If possible, avoid direct sunlight and store in cool and area of low humidity

2)In order to maintain the quality of the product and avoid misuse

3)Avoid placing the product near fire and store out in reach of children

DOSAGE & ADMINISTRATION SECTION

for external use only


PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70845-0010-12020-01-31C16284748780-19d75b9d0-fd09-f424-e053-dadaa90a57ceDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70845-0010-1UNDA HAIR MOISTURIZING250 mL in 1 BOTTLE, PUMPCREAM2501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70845-0010UNDA HAIR MOISTURIZING (BAMBUSA VULGARIS EXTRACT, SHEA BUTTER, EUCALYPTUS GLOBULUS LEAF OIL) CREAM [UNDA]1Legacy NDC, 1 package rows20160725_386db1d4-3d9f-223b-e054-00144ff8d46c.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70845-001070845-0010-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

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
386db1d4-3da0-223b-e054-00144ff8d46c386db1d4-3d9f-223b-e054-00144ff8d46c2016-07-24WarningsExact identifier
spl id: 386db1d4-3da0-223b-e054-00144ff8d46c
spl set id: 386db1d4-3d9f-223b-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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