ManiMe MOISTURIZING HAND SANITIZER

Manufacturer
Cospharm Co.,Ltd
Effective date
2022-03-09
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:06:41

Label at a glance#

ProductManiMe MOISTURIZING HAND SANITIZER
Active ingredientALCOHOL
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Inner containerInner containerOuter boxOuter box

WARNINGS SECTION

OTC - ACTIVE INGREDIENT SECTION

INACTIVE INGREDIENT SECTION

DOSAGE & ADMINISTRATION SECTION

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

OTC - DO NOT USE SECTION

OTC - PURPOSE SECTION

OTC - STOP USE SECTION

INDICATIONS & USAGE SECTION

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
75681-670-022022-03-09C16284748780-1d6a99b39-8ca7-a426-e053-dadaa90af4c275681-670-02 ManiMe MOISTURIZING HAND SANITIZER
75681-670-022022-01-28C16284748780-1d6a99b39-8ca7-a426-e053-dadaa90af4c275681-670-02 ManiMe MOISTURIZING HAND SANITIZER

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75681-67075681-670-01, 75681-670-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 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
0317bca2-47f9-3016-e063-6394a90a802ea6fc4b83-bac0-5004-e053-2995a90a8e1f2023-08-17Exact identifier
spl set id: a6fc4b83-bac0-5004-e053-2995a90a8e1f

Reported adverse events (FAERS/openFDA)#

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