A and D

Manufacturer
H&H Laboratories, Inc.
Effective date
2012-05-14
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:32:01

Label at a glance#

ProductA and D
Active ingredientPETROLATUM
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient (in each gram): White Petrolatum 93.5%

OTC - PURPOSE SECTION

Purpose-Skin Protectant

INDICATIONS & USAGE SECTION

Uses-Temporarily protects minor cuts, scrapes, and sunburn.     Temporarily protects and helps chapped or cracked skin and lips.  Helps protect lips from drying effects of wind and cold weather.

DOSAGE & ADMINISTRATION SECTION

Directions: Apply liberally as needed  Change wet and soiled diapers promptly.  Cleanse the diaper area and allow to dry. Use with each diaper change, especially at bedtime when exposure to wet diapers may be prolonged.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.  If swallowed, get medical help or contact a Poison Control Center right away.

WARNINGS SECTION

For external use only.  Avoid contact with eyes.  on deep puncture wounds, animal bites, or serious burns.

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

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Corn Oil, Light Mineral Oil, Vitamin A Palmitate, Vitamin D

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

MM1


H and H AD Carton.jpgH and H AD Carton.jpg



DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
a1367f07-14a3-4895-a6e7-61ee9285308bProduct name120190415

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
52471-101-472019-11-13C16284748780-197449f38-b738-f6ea-e053-dbdaa90aa703DRUG FACTS

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
52471-101-05A and D5 g in 1 PACKETOINTMENT51
52471-101-47A and D144 in 1 CARTONOINTMENT1441

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
52471-101A AND D (PETROLATUM) OINTMENT [H&H LABORATORIES, INC.]1Legacy NDC, 2 package rows20120523_00bc354f-9f7b-4288-9bbe-a140a6643d20.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
PETROLATUMACTIVE INGREDIENT4T6H12BN9U1
PETROLATUMACTIVE MOIETY4T6H12BN9U1
ERGOCALCIFEROLINACTIVE INGREDIENTVS041H42XC1
VITAMIN A PALMITATEINACTIVE INGREDIENT1D1K0N0VVC1

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
52471-10152471-101-05, 52471-101-47

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 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
41f08daa-55b1-42ac-b2e2-4a8dd888353600bc354f-9f7b-4288-9bbe-a140a6643d202012-05-14WarningsExact identifier
spl id: 41f08daa-55b1-42ac-b2e2-4a8dd8883536
spl set id: 00bc354f-9f7b-4288-9bbe-a140a6643d20

Reported adverse events (FAERS/openFDA)#

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