Lantiseptic Dry Skin Therapy

Manufacturer: Dermarite Industries LLC | Dermarite Industires LLC
Effective date: 2024-12-05
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: full-release
Hydrated at: 2026-06-01 00:40:56

Label at a glance#

ProductLantiseptic Dry Skin Therapy

Active ingredientLANOLIN

Label structure8 sections

Indications and uses

Temporarily protects minor cuts, scrapes, and burns Helps prevent and temporarily protects chafed, chapped, or cracked skin.

Dosage and administration

Apply liberally to affected area as needed or as directed by a physician.

Contacts and useful links#

PhoneLabel contact1-800-337-6296

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Lanolin USP 30%

Purpose

OTC - PURPOSE SECTION

Skin Protectant

Uses

INDICATIONS & USAGE SECTION

Temporarily protects minor cuts, scrapes, and burns
Helps prevent and temporarily protects chafed, chapped, or cracked skin.

Warnings

WARNINGS SECTION

• For external use only. • Avoid contact with eyes. •In case of contact, flush thoroughly with water.

Do not use on

deep or puncture wounds
animal bites
serious burns

Stop use and ask a doctor if

conditions worsen
symptoms last more than 7 days or clear up and occur again within a few days.

Keep our of reach of children

In case of accidental ingestion contact a physician or Poison Control Center right away.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Directions

DOSAGE & ADMINISTRATION SECTION

Apply liberally to affected area as needed or as directed by a physician.

Other Information

SPL UNCLASSIFIED SECTION

Store at room temperature (59-86°F)
You may report a serious adverse event to DermaRite Industries, PO Box 7209, North Bergen, NJ07047

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Mineral Oil, Petrolatum, Cera Alba, Sodium Borate, DMDM Hydantoin, Sorbitan Sesquioleate, Lanolin Alcohol, Disodium EDTA

Questions or Comments?

OTC - QUESTIONS SECTION

Call 1-800-337-6296 Mon-Fri 9AM-5PM EST.

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Principal packaging display

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1657183	lanolin 30 % Topical Cream	PSN	3
1657185	Lantiseptic 30 % Topical Cream	PSN	3
1657185	lanolin 300 MG/ML Topical Cream [Lantiseptic]	SBD	3
1657183	lanolin 300 MG/ML Topical Cream	SCD	3
1657183	lanolin 30 % Topical Cream	SY	3
1657185	Lantiseptic 30 % Topical Cream	SY	3
1657185	Lantiseptic 300 MG/ML Topical Cream	SY	3

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
61924-710-14	2024-12-06	C162847	48780-1	d6a99b39-ba22-a426-e053-dadaa90af4c2	Lantiseptic by Dermarite Daily Care Skin Protectant
61924-710-14	2022-01-28	C162847	48780-1	d6a99b39-ba22-a426-e053-dadaa90af4c2	Lantiseptic by Dermarite Daily Care Skin Protectant

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
61924-710-14	Lantiseptic Dry Skin Therapy	397 g in 1 JAR	CREAM	397		3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
61924-710	LANTISEPTIC DRY SKIN THERAPY (LANOLIN) CREAM [DERMARITE INDUSTRIES LLC]	3	Legacy NDC, 1 package rows	20241208_77316878-e79d-fba3-e053-2a91aa0a9391.zip

Products#

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

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

Lantiseptic Dry Skin Therapy
LANOLIN
YELLOW WAX
EDETATE DISODIUM
LANOLIN ALCOHOLS
MINERAL OIL
PETROLATUM
WATER
SODIUM BORATE
SORBITAN SESQUIOLEATE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
61924-710	61924-710-14

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
Name	UNII	Kind
YELLOW WAX	2ZA36H0S2V	IACT
EDETATE DISODIUM	7FLD91C86K	IACT
LANOLIN ALCOHOLS	884C3FA9HE	IACT
MINERAL OIL	T5L8T28FGP	IACT
PETROLATUM	4T6H12BN9U	IACT
WATER	059QF0KO0R	IACT
SODIUM BORATE	91MBZ8H3QO	IACT
SORBITAN SESQUIOLEATE	0W8RRI5W5A	IACT
LANOLIN	7EV65EAW6H	ACTIB

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
288a202f-149d-208c-e063-6394a90a90c5			77316878-e79d-fba3-e053-2a91aa0a9391	2024-12-05	Warnings	Exact identifier spl id: 288a202f-149d-208c-e063-6394a90a90c5 spl set id: 77316878-e79d-fba3-e053-2a91aa0a9391

Reported adverse events (FAERS/openFDA)#

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