UNDA MOSITURIZING

Manufacturer
UNDA
Effective date
2016-07-25
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:46:36

Label at a glance#

ProductUNDA MOSITURIZING
Active ingredientSALICYLIC ACID, EUCALYPTUS GLOBULUS LEAF, BAMBUSA VULGARIS TOP
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Salicylic Acid, Bambusa Vulgaris Extract, Eucalyptus Globulus Leaf Oil

INACTIVE INGREDIENT SECTION

Cocamidopropyl Betaine, TEA-Cocoyl Glutamate, Disodium Cocoamphodiacetate, Glycerin, PEG-150 Distearate, Behentrimonium Chloride, Caprylyl Glycol, Niacinamide, Sciadopitys Verticillata Root Extract, Krameria Triandra Root Extract, Decylene Glycol, Ethylhexylglycerin, Hexylene Glycol, Butylene Glycol, Totarol, Tocopheryl Acetate, Retinyl Palmitate, Allantoin, Phenylalanine, Proline, Threonine, Tryptophan, Valine, Pyridoxine, Ascorbic Acid, Polyquaternium-10

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 one pump of Ünda moisturizing shampoo.
  3. Using the tip of your fingertips, rub the shampoo into your hair and make plenty of bubbles.
  4. Enjoy its natural scent and massage your scalp for 2~3 minutes
  5. Wash off with lukewarm water
  6. Dry your hair with a dry towel
  7. 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

ll

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
dea2eded-d1e7-46bb-9a3d-f8dc20de6277Product name120190408

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70845-0011-12020-01-31C16284748780-19d75b9d0-4ca2-f424-e053-dadaa90a57ceDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70845-0011-1UNDA MOSITURIZING500 mL in 1 BOTTLE, PUMPSHAMPOO5001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70845-0011UNDA MOSITURIZING (SALICYLIC ACID, BAMBUSA VULGARIS EXTRACT, EUCALYPTUS GLOBULUS LEAF OIL) SHAMPOO [UNDA]1Legacy NDC, 1 package rows20160725_386db1d4-3da5-223b-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
70845-001170845-0011-1

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
386db1d4-3da6-223b-e054-00144ff8d46c386db1d4-3da5-223b-e054-00144ff8d46c2016-07-25WarningsExact identifier
spl id: 386db1d4-3da6-223b-e054-00144ff8d46c
spl set id: 386db1d4-3da5-223b-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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