Daily Moisturizing Lotion

Manufacturer: Donegal Bay Ltd | HANGZHOU KARIC COMMODITIES CO., LTD
Effective date: 2016-10-12
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 22:47:39

Label at a glance#

ProductFootscriptions Foot Repair

Active ingredientMENTHOL

Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient:

Menthol USP 0.1%

OTC - PURPOSE SECTION

Purpose:

External Analgesic

INDICATIONS & USAGE SECTION

Uses:

Temporarily relieves pain and itching associated with skin irritations

WARNINGS SECTION

Warnings:

For external use only

When using this product, avoid contacting with eyes

OTC - STOP USE SECTION

Stop use and ask a doctor if condition worsens or if symptoms last for more than 7 days or clear up and occur again within a few days

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of accidental ingestion, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

Direction:

Adults and children 2 years and older: apply up to 3-4 times daily.

Under 2 years: ask a doctor

Wash and dry feet, apply liberally over feet, between toes, on bottoms of feet, and message until absorbed.

INACTIVE INGREDIENT SECTION

Inactive Ingredients:

Aloe Barbadenis Leaf Juice, Water, Mineral Oil, Glycerryl Stearate, PEG-100 Stearate, Cetyl Alcohol, Cetearyl Alcohol, Polysorbate 60, Propylene Glycol, Stearic Acid, Hydrogenated Polyisobutene, Dimethicone, Triethanolamine, Salicylic Acid, Imidazlidinyl, Urea, Chondrus Crispus, Methylparaben, Propylparaben, Mentha Piperita (peppermint) Oil, Chloroxylenol, DMDM Hydantoin

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
200066	menthol 0.1 % Topical Cream	PSN	1
200066	menthol 1 MG/ML Topical Cream	SCD	1
200066	menthol 0.1 % Topical Cream	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
70990-002-01	2020-01-31	C162847	48780-1	9d75b9cf-de08-f424-e053-dadaa90a57ce	Daily Moisturizing Lotion

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
70990-002-01	Footscriptions Foot Repair	252 mL in 1 TUBE	CREAM	252		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
70990-002	FOOTSCRIPTIONS FOOT REPAIR (MENTHOL) CREAM [DONEGAL BAY LTD]	1	Legacy NDC, 1 package rows	20161017_aa33d301-a56c-4519-a044-d56b53c7205c.zip

Products#

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

DailyMed product names page 1 of 1 · 21 matching rows.

Footscriptions Foot Repair
MENTHOL
WATER
ALOE ANDONGENSIS LEAF
CETYL ALCOHOL
MINERAL OIL
GLYCERYL STEARATE SE
PEG-100 STEARATE
POLYSORBATE 60
PROPYLENE GLYCOL
STEARIC ACID
HYDROGENATED POLYBUTENE (1300 MW)
DIMETHICONE
SALICYLIC ACID
UREA
CHONDRUS CRISPUS
METHYLPARABEN
PROPYLPARABEN
PEPPERMINT OIL
CHLOROXYLENOL
DMDM HYDANTOIN

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
70990-002	70990-002-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 20 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
MENTHOL	L7T10EIP3A	ACTIB
ALOE ANDONGENSIS LEAF	N1P4NU25EJ	IACT
CETYL ALCOHOL	936JST6JCN	IACT
MINERAL OIL	T5L8T28FGP	IACT
GLYCERYL STEARATE SE	FCZ5MH785I	IACT
PEG-100 STEARATE	YD01N1999R	IACT
POLYSORBATE 60	CAL22UVI4M	IACT
PROPYLENE GLYCOL	6DC9Q167V3	IACT
STEARIC ACID	4ELV7Z65AP	IACT
HYDROGENATED POLYBUTENE (1300 MW)	7D1YQ9Y5EZ	IACT
DIMETHICONE	92RU3N3Y1O	IACT
SALICYLIC ACID	O414PZ4LPZ	IACT
UREA	8W8T17847W	IACT
CHONDRUS CRISPUS	OQS23HUA1X	IACT
METHYLPARABEN	A2I8C7HI9T	IACT
PROPYLPARABEN	Z8IX2SC1OH	IACT
PEPPERMINT OIL	AV092KU4JH	IACT
CHLOROXYLENOL	0F32U78V2Q	IACT
DMDM HYDANTOIN	BYR0546TOW	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
f64728fc-302c-4e7f-9df7-5448cd7fa67f			aa33d301-a56c-4519-a044-d56b53c7205c	2016-10-12	Warnings	Exact identifier spl id: f64728fc-302c-4e7f-9df7-5448cd7fa67f spl set id: aa33d301-a56c-4519-a044-d56b53c7205c

Reported adverse events (FAERS/openFDA)#

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