Dermadrox Ointment

Manufacturer: GERITREX LLC
Effective date: 2016-10-20
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: full-release
Hydrated at: 2026-05-31 22:47:53

Label at a glance#

ProductDermadrox

Active ingredientALUMINUM HYDROXIDE

Label structure9 sections

Storage and handling

Store at room temperature (59'F-86'F) Keep lid tightly closed

Label contents#

Full prescribing information#

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients Purpose

Aluminum Hydroxide Gel A skin protectant

Intended Use

OTC - PURPOSE SECTION

Used for relief of minor skin irritations such as chafing, Interigo and galling

Provides temporary relief to abraded skin, friction burns and rubbing

Lubricates effectively on psoriatic skin

Effective for dried cracked skin, sunburn and abraded skin

Warnings

WARNINGS SECTION

For External Use Only

Avoid contact with eyes

Discontinue use if symptoms persist for more than 7 days

DERMADROX ointment is contraindicated in patients with a history of hypersensitivity to any of its components

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Calcium Carbonate, Citric Acid, Deionized Water, Glycerin, Lanolin, Lanolin Alcohol, Magnesium Hydroxide, Mineral Oil,

Petrolatum, Sodium Chloride, Sodium Laureth Sulfate, Stearyl Alcohol, Vitamin A and D, Zinc Chloride

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

Storage

STORAGE AND HANDLING SECTION

Store at room temperature (59'F-86'F) Keep lid tightly closed

DOSAGE & ADMINISTRATION SECTION

Reapply at least every 12 hours

Direction

INDICATIONS & USAGE SECTION

Apply liberally as often as necessary to minor burns, abraded skin, irritated areas and minor wounds

Reapply at least every 12 hours

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1368022	aluminum hydroxide 1.2 % Topical Ointment	PSN	3
1368022	aluminum hydroxide 0.012 MG/MG Topical Ointment	SCD	3
1368022	aluminum hydroxide 1.2 % Topical Ointment	SY	3

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
030ce964-9b2d-45aa-b5d3-f78ce03ef61c	Product name	2	20250515

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
54162-221-04	2020-01-31	C162847	48780-1	9d75b9d0-e587-f424-e053-dadaa90a57ce	Dermadrox Ointment

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
54162-221-04	Dermadrox	113 g in 1 JAR	OINTMENT	113		3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
54162-221	DERMADROX (ALUMINUM HYDROXIDE) OINTMENT [GERITREX LLC]	3	Legacy NDC, 1 package rows	20161103_dcf0aa6c-5fe7-46e3-a418-c79ecaca074c.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
54162-221-01	GM - Gram	54162-221	a6eef10b-e111-48a4-ba7d-54911ab23329	1	2013-03-03
54162-221-04	GM - Gram	54162-221	34c84eb2-751d-45cf-a5c5-18f6a1cf0648	1	2013-11-04

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
ALUMINUM HYDROXIDE	ACTIVE INGREDIENT	5QB0T2IUN0	2
ALUMINUM HYDROXIDE	ACTIVE MOIETY	5QB0T2IUN0	2
CALCIUM CARBONATE	INACTIVE INGREDIENT	H0G9379FGK	2
CITRIC ACID ACETATE	INACTIVE INGREDIENT	DSO12WL7AU	2
GLYCERIN	INACTIVE INGREDIENT	PDC6A3C0OX	2
LANOLIN	INACTIVE INGREDIENT	7EV65EAW6H	2
LANOLIN ALCOHOLS	INACTIVE INGREDIENT	884C3FA9HE	2
MAGNESIUM HYDROXIDE	INACTIVE INGREDIENT	NBZ3QY004S	2
MINERAL OIL	INACTIVE INGREDIENT	T5L8T28FGP	2
PETROLATUM	INACTIVE INGREDIENT	4T6H12BN9U	2
SODIUM CHLORIDE	INACTIVE INGREDIENT	451W47IQ8X	2
SODIUM LAURETH SULFATE	INACTIVE INGREDIENT	BPV390UAP0	2
STEARYL ALCOHOL	INACTIVE INGREDIENT	2KR89I4H1Y	2
VITAMIN A	INACTIVE INGREDIENT	81G40H8B0T	2
VITAMIN D	INACTIVE INGREDIENT	9VU1KI44GP	2
WATER	INACTIVE INGREDIENT	059QF0KO0R	2
ZINC CHLORIDE	INACTIVE INGREDIENT	86Q357L16B	2

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

Dermadrox
Aluminum Hydroxide
CALCIUM CARBONATE
CITRIC ACID ACETATE
WATER
GLYCERIN
LANOLIN
LANOLIN ALCOHOLS
MAGNESIUM HYDROXIDE
MINERAL OIL
PETROLATUM
SODIUM CHLORIDE
SODIUM LAURETH SULFATE
STEARYL ALCOHOL
VITAMIN A
VITAMIN D
ZINC CHLORIDE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
54162-221	54162-221-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 16 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ALUMINUM HYDROXIDE	5QB0T2IUN0	ACTIB
CALCIUM CARBONATE	H0G9379FGK	IACT
CITRIC ACID ACETATE	DSO12WL7AU	IACT
WATER	059QF0KO0R	IACT
GLYCERIN	PDC6A3C0OX	IACT
LANOLIN	7EV65EAW6H	IACT
LANOLIN ALCOHOLS	884C3FA9HE	IACT
MAGNESIUM HYDROXIDE	NBZ3QY004S	IACT
MINERAL OIL	T5L8T28FGP	IACT
PETROLATUM	4T6H12BN9U	IACT
SODIUM CHLORIDE	451W47IQ8X	IACT
SODIUM LAURETH SULFATE	BPV390UAP0	IACT
STEARYL ALCOHOL	2KR89I4H1Y	IACT
VITAMIN A	81G40H8B0T	IACT
VITAMIN D	9VU1KI44GP	IACT
ZINC CHLORIDE	86Q357L16B	IACT

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 6 · 313 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredient	IID ingredient	UNII	Dosage form / route	Potency	Maximum daily exposure	Match
SODIUM CHLORIDE	SODIUM CHLORIDE	451W47IQ8X	INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION / INTRAMUSCULAR		360 mg	Exact identifier — unii candidate 134 equally ranked IID candidates
SODIUM CHLORIDE	SODIUM CHLORIDE	451W47IQ8X	INJECTION, SUSPENSION / INTRA-ARTICULAR		26 mg	Exact identifier — unii candidate 134 equally ranked IID candidates
SODIUM CHLORIDE	SODIUM CHLORIDE	451W47IQ8X	INJECTION / INTRACAVITARY	0.82 %w/v		Exact identifier — unii candidate 134 equally ranked IID candidates
GLYCERIN	GLYCERIN	PDC6A3C0OX	JELLY / VAGINAL	NA		Exact identifier — unii candidate 75 equally ranked IID candidates
ZINC CHLORIDE	ZINC CHLORIDE	86Q357L16B	INJECTION / INTRADERMAL	7 mg		Exact identifier — unii candidate 5 equally ranked IID candidates
SODIUM CHLORIDE	SODIUM CHLORIDE	451W47IQ8X	SUSPENSION / ENDOTRACHEAL	7.6 mg		Exact identifier — unii candidate 134 equally ranked IID candidates
GLYCERIN	GLYCERIN	PDC6A3C0OX	TABLET / ORAL		42 mg	Exact identifier — unii candidate 75 equally ranked IID candidates
SODIUM CHLORIDE	SODIUM CHLORIDE	451W47IQ8X	LIQUID / SUBCUTANEOUS	0.7 %w/v		Exact identifier — unii candidate 134 equally ranked IID candidates
SODIUM CHLORIDE	SODIUM CHLORIDE	451W47IQ8X	INJECTION, SOLUTION / INTRAVESICAL		351 mg	Exact identifier — unii candidate 134 equally ranked IID candidates
GLYCERIN	GLYCERIN	PDC6A3C0OX	SYSTEM / TOPICAL		18144 mg	Exact identifier — unii candidate 75 equally ranked IID candidates
SODIUM CHLORIDE	SODIUM CHLORIDE	451W47IQ8X	SOLUTION / INTRAVENOUS		90 mg	Exact identifier — unii candidate 134 equally ranked IID candidates
SODIUM CHLORIDE	SODIUM CHLORIDE	451W47IQ8X	INJECTION / PARENTERAL		584 mg	Exact identifier — unii candidate 134 equally ranked IID candidates
PETROLATUM	PETROLATUM	4T6H12BN9U	AEROSOL, FOAM / TOPICAL	7.9 %w/w		Exact identifier — unii candidate 18 equally ranked IID candidates
STEARYL ALCOHOL	STEARYL ALCOHOL	2KR89I4H1Y	POWDER / ORAL	0.11 mg		Exact identifier — unii candidate 12 equally ranked IID candidates
PETROLATUM	PETROLATUM	4T6H12BN9U	OINTMENT, AUGMENTED / TOPICAL	81.94 %w/w		Exact identifier — unii candidate 18 equally ranked IID candidates
MINERAL OIL	MINERAL OIL	T5L8T28FGP	PASTE / DENTAL	95 %w/w		Exact identifier — unii candidate 30 equally ranked IID candidates
SODIUM CHLORIDE	SODIUM CHLORIDE	451W47IQ8X	INJECTION / PERINEURAL		648 mg	Exact identifier — unii candidate 134 equally ranked IID candidates
SODIUM CHLORIDE	SODIUM CHLORIDE	451W47IQ8X	SPRAY, METERED / NASAL		36 mg	Exact identifier — unii candidate 134 equally ranked IID candidates
LANOLIN ALCOHOLS	LANOLIN ALCOHOLS	884C3FA9HE	OINTMENT / TOPICAL		452 mg	Exact identifier — unii candidate 4 equally ranked IID candidates
STEARYL ALCOHOL	STEARYL ALCOHOL	2KR89I4H1Y	SUSPENSION / TOPICAL	2.01 %w/w		Exact identifier — unii candidate 12 equally ranked IID candidates
LANOLIN ALCOHOLS	LANOLIN ALCOHOLS	884C3FA9HE	LOTION / TOPICAL		9360 mg	Exact identifier — unii candidate 4 equally ranked IID candidates
SODIUM CHLORIDE	SODIUM CHLORIDE	451W47IQ8X	INJECTION / SUBMUCOSAL		17 mg	Exact identifier — unii candidate 134 equally ranked IID candidates
STEARYL ALCOHOL	STEARYL ALCOHOL	2KR89I4H1Y	TABLET, EXTENDED RELEASE / ORAL	244 mg		Exact identifier — unii candidate 12 equally ranked IID candidates
SODIUM CHLORIDE	SODIUM CHLORIDE	451W47IQ8X	IMPLANT / SUBCUTANEOUS	77 mg		Exact identifier — unii candidate 134 equally ranked IID candidates
PETROLATUM	PETROLATUM	4T6H12BN9U	EMULSION / TOPICAL	7.8 %w/w		Exact identifier — unii candidate 18 equally ranked IID candidates
SODIUM CHLORIDE	SODIUM CHLORIDE	451W47IQ8X	INJECTION / INTRA-ARTERIAL		278 mg	Exact identifier — unii candidate 134 equally ranked IID candidates
SODIUM CHLORIDE	SODIUM CHLORIDE	451W47IQ8X	INJECTION / INTRACAUDAL		210 mg	Exact identifier — unii candidate 134 equally ranked IID candidates
SODIUM CHLORIDE	SODIUM CHLORIDE	451W47IQ8X	SOLUTION / ORAL		148 mg	Exact identifier — unii candidate 134 equally ranked IID candidates
MINERAL OIL	MINERAL OIL	T5L8T28FGP	OINTMENT / OPHTHALMIC	59.5 %w/w		Exact identifier — unii candidate 30 equally ranked IID candidates
SODIUM CHLORIDE	SODIUM CHLORIDE	451W47IQ8X	DROPS / OPHTHALMIC	0.08 %w/w		Exact identifier — unii candidate 134 equally ranked IID candidates
LANOLIN ALCOHOLS	LANOLIN ALCOHOLS	884C3FA9HE	CREAM / TOPICAL	6 %w/w		Exact identifier — unii candidate 4 equally ranked IID candidates
MAGNESIUM HYDROXIDE	MAGNESIUM HYDROXIDE	NBZ3QY004S	TABLET / ORAL		120 mg	Exact identifier — unii candidate 6 equally ranked IID candidates
SODIUM CHLORIDE	SODIUM CHLORIDE	451W47IQ8X	SUSPENSION / SUBCUTANEOUS	0.8 %w/v		Exact identifier — unii candidate 134 equally ranked IID candidates
SODIUM CHLORIDE	SODIUM CHLORIDE	451W47IQ8X	INJECTION, SOLUTION / INTRAVENOUS		2916 mg	Exact identifier — unii candidate 134 equally ranked IID candidates
SODIUM CHLORIDE	SODIUM CHLORIDE	451W47IQ8X	SOLUTION/ DROPS / OPHTHALMIC		55 mg	Exact identifier — unii candidate 134 equally ranked IID candidates
GLYCERIN	GLYCERIN	PDC6A3C0OX	CREAM / TOPICAL		1720 mg	Exact identifier — unii candidate 75 equally ranked IID candidates
STEARYL ALCOHOL	STEARYL ALCOHOL	2KR89I4H1Y	CREAM / VAGINAL		425 mg	Exact identifier — unii candidate 12 equally ranked IID candidates
CALCIUM CARBONATE	CALCIUM CARBONATE	H0G9379FGK	TABLET, CHEWABLE / ORAL		1650 mg	Exact identifier — unii candidate 15 equally ranked IID candidates
SODIUM CHLORIDE	SODIUM CHLORIDE	451W47IQ8X	INJECTION / SUBCUTANEOUS		1486 mg	Exact identifier — unii candidate 134 equally ranked IID candidates
MINERAL OIL	MINERAL OIL	T5L8T28FGP	DROPS / ORAL	NA		Exact identifier — unii candidate 30 equally ranked IID candidates
SODIUM CHLORIDE	SODIUM CHLORIDE	451W47IQ8X	INJECTION, SUSPENSION, LIPOSOMAL / EPIDURAL		11 mg	Exact identifier — unii candidate 134 equally ranked IID candidates
SODIUM CHLORIDE	SODIUM CHLORIDE	451W47IQ8X	SOLUTION / OPHTHALMIC		13 mg	Exact identifier — unii candidate 134 equally ranked IID candidates
PETROLATUM	PETROLATUM	4T6H12BN9U	CREAM, AUGMENTED / TOPICAL	26 %w/w		Exact identifier — unii candidate 18 equally ranked IID candidates
SODIUM CHLORIDE	SODIUM CHLORIDE	451W47IQ8X	INJECTION / ENDOTRACHEAL		68 mg	Exact identifier — unii candidate 134 equally ranked IID candidates
GLYCERIN	GLYCERIN	PDC6A3C0OX	TABLET / PERIODONTAL	0.53 mg		Exact identifier — unii candidate 75 equally ranked IID candidates
GLYCERIN	GLYCERIN	PDC6A3C0OX	INJECTION, EMULSION / INTRAVENOUS		24100 mg	Exact identifier — unii candidate 75 equally ranked IID candidates
GLYCERIN	GLYCERIN	PDC6A3C0OX	INJECTION / INTRAMUSCULAR		450 mg	Exact identifier — unii candidate 75 equally ranked IID candidates
MINERAL OIL	MINERAL OIL	T5L8T28FGP	CAPSULE, EXTENDED RELEASE / ORAL		120 mg	Exact identifier — unii candidate 30 equally ranked IID candidates
LANOLIN	LANOLIN	7EV65EAW6H	SHAMPOO / TOPICAL	2 %w/w		Exact identifier — unii candidate 9 equally ranked IID candidates
LANOLIN ALCOHOLS	LANOLIN ALCOHOLS	884C3FA9HE	OINTMENT / OPHTHALMIC	10 %w/w		Exact identifier — unii candidate 4 equally ranked IID candidates
GLYCERIN	GLYCERIN	PDC6A3C0OX	SYRUP / ORAL		16734 mg	Exact identifier — unii candidate 75 equally ranked IID candidates
CALCIUM CARBONATE	CALCIUM CARBONATE	H0G9379FGK	TABLET / ORAL		793 mg	Exact identifier — unii candidate 15 equally ranked IID candidates
GLYCERIN	GLYCERIN	PDC6A3C0OX	INJECTION, SUSPENSION / SUBCUTANEOUS	1.6 %w/v		Exact identifier — unii candidate 75 equally ranked IID candidates
LANOLIN	LANOLIN	7EV65EAW6H	CREAM / TOPICAL		10 mg	Exact identifier — unii candidate 9 equally ranked IID candidates
PETROLATUM	PETROLATUM	4T6H12BN9U	TABLET / ORAL	3.5 mg		Exact identifier — unii candidate 18 equally ranked IID candidates
SODIUM CHLORIDE	SODIUM CHLORIDE	451W47IQ8X	INJECTION / INTRAVENOUS		28773 mg	Exact identifier — unii candidate 134 equally ranked IID candidates
SODIUM CHLORIDE	SODIUM CHLORIDE	451W47IQ8X	INJECTION, SOLUTION / SUBMUCOSAL	16 %w/v		Exact identifier — unii candidate 134 equally ranked IID candidates
SODIUM CHLORIDE	SODIUM CHLORIDE	451W47IQ8X	INJECTION / PERIDURAL	8.07 mg		Exact identifier — unii candidate 134 equally ranked IID candidates
GLYCERIN	GLYCERIN	PDC6A3C0OX	CLOTH / TOPICAL	0.05 mg/mg		Exact identifier — unii candidate 75 equally ranked IID candidates
SODIUM CHLORIDE	SODIUM CHLORIDE	451W47IQ8X	INJECTION / INTRATHECAL		9 mg	Exact identifier — unii candidate 134 equally ranked IID candidates

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
31e3fc58-0d5f-492f-b1f7-2e738c51a7f9			dcf0aa6c-5fe7-46e3-a418-c79ecaca074c	2016-10-20	Warnings	Exact identifier spl id: 31e3fc58-0d5f-492f-b1f7-2e738c51a7f9 spl set id: dcf0aa6c-5fe7-46e3-a418-c79ecaca074c

Reported adverse events (FAERS/openFDA)#

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