186 Curad Vitamin A&D ointment

Manufacturer: Medline Industries, LP
Effective date: 2025-11-04
Label type: HUMAN OTC DRUG LABEL
Version: 4
Source: full-release
Hydrated at: 2026-06-01 01:42:11

Label at a glance#

ProductMedline

Active ingredientWHITE PETROLATUM

Label structure9 sections

Indications and uses

temporarily protects and relieves minor cuts scrapes burns chapped or cracked skin and lips

Dosage and administration

apply as needed

Contacts and useful links#

PhoneLabel contact1-800-633-5463

Websitewww.curad.com

www.curad.com

Label contents#

Full prescribing information#

Active ingredient (in each gram)

OTC - ACTIVE INGREDIENT SECTION

White petrolatum 93.4%, USP

Purpose

OTC - PURPOSE SECTION

Skin protectant

Uses

INDICATIONS & USAGE SECTION

temporarily protects and relieves
minor cuts
scrapes
burns
chapped or cracked skin and lips

Warnings

WARNINGS SECTION

for external use only

Do not use on

OTC - DO NOT USE SECTION

deep or puncture wounds
animal bites
serious burns

When using this product

OTC - WHEN USING SECTION

do not get into eyes

Stop use and ask a doctor if

OTC - STOP USE SECTION

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

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

apply as needed

Other information

OTHER SAFETY INFORMATION

store at controlled room temperature 68-77°F (20-25°C)
use only if packaging is intact

Inactive ingredients

INACTIVE INGREDIENT SECTION

lavender oil, light mineral oil, vitamin A palmitate, vitamin D

Manufacturing Information

SPL UNCLASSIFIED SECTION

Made in India

Manufactured for Medline Industries, LP

Three Lakes Drive, Northfield, IL 60093 USA

Visit us at www.curad.com or call: 1-800-633-5463

REF: CUR003501

53329-186-14 Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

53329-186-14_RB23GZP

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
2601369	petrolatum 93.4 % Topical Ointment	PSN	4
2601369	petrolatum 0.934 MG/MG Topical Ointment	SCD	4

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
53329-186-14	Medline	1 in 1 BOX	OINTMENT	1	4
53329-186-14	Medline	56.6 g in 1 TUBE	OINTMENT	56.6	4
53329-186-16	Medline	5 g in 1 PACKET	OINTMENT	5	4
53329-186-96	Medline	144 in 1 BOX	OINTMENT	144	4

Products#

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

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

Medline
petrolatum
LIGHT MINERAL OIL
VITAMIN A PALMITATE
VITAMIN D
LAVENDER OIL
WHITE PETROLATUM

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
53329-186	53329-186-16, 53329-186-96, 53329-186-14

Ingredients#

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

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

Name, UNII, Kind table
Name	UNII	Kind
LIGHT MINERAL OIL	N6K5787QVP	IACT
VITAMIN A PALMITATE	1D1K0N0VVC	IACT
VITAMIN D	9VU1KI44GP	IACT
LAVENDER OIL	ZBP1YXW0H8	IACT
WHITE PETROLATUM	B6E5W8RQJ4	ACTIB

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
Version	Effective date	Source	Hydrated
3	2024-12-04	full-release	2026-06-01 00:40:42

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
Medline	PETROLATUM	Medline Industries, LP	f3062b61-e4c4-9f57-e053-2995a90aa028	2025-11-04	Warnings	Exact identifier ndc (package): 53329-186-14 ndc (package): 53329-186-16 ndc (package): 53329-186-96 ndc (product): 53329-186 ndc11 (package): 53329018614 ndc11 (package): 53329018696 ndc11 (package): 53329018616 spl id: 42c7c6aa-dac4-0498-e063-6394a90a3516 spl set id: f3062b61-e4c4-9f57-e053-2995a90aa028

Reported adverse events (FAERS/openFDA)#

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