Always my Baby 020.002/020AC-AD Diaper Rash Ointment 40% Zinc Oxide

Zinc Oxide by

Drug Labeling and Warnings

Zinc Oxide by is a Otc medication manufactured, distributed, or labeled by AHOLD U.S.A., INC., Vi Jon, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ZINC OXIDE- zinc oxide ointment 
AHOLD U.S.A., INC.

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Always my Baby 020.002/020AC-AD
Diaper Rash Ointment 40% Zinc Oxide

Active ingredient

Zinc oxide  40%

Purpose

Skin Protectant

Uses

helps treat and prevent diaper rash
protects chafed skin due to the diaper rash and helps seal out wetness

Warnings

For external use only

When using this product

• do not get into eyes

Stop use and ask a doctor if

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

Keep out of reach of children.

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

Directions

change wet and soiled diapers promptly
cleanse the diaper area
allow to dry
apply ointment liberally as often as necessary, with each diaper change, especially at bedtime or anytime when exposure to wet diapers may be prolonged

Other information

store between 20⁰ and 25⁰C (68⁰ and 77⁰F)

Inactive ingredients

petrolatum, cod liver oil, lanolin, Zea mays (corn) starch, glycerin, sorbitan sesquioleate, beeswax, tocopheryl acetate, fragrance

*This Always My Baby Diaper Rash Ointment is not manufactured or distributed by Johnson & Johnson Consumer Products Company, distibutor of Desitin Maximum Strength 40% Zinc Oxide Diaper Rash Paste.

Distributed By: 

ADUSA DISTRIBUTION, LLC

SALISBURY, NC 28147

For product questions or concerns, contact us at 1-833992-3872

Quality guaranteed or your money back.

Compare to Desitin Maximum Strength 40% Zinc Oxide Diaper Rash Paste*

40% zinc

diaper rash ointment

• helps to heal, soothe & prevent diaper rash
• no paraben
• this product does not contain talc
• hypoallergenic
• pediatrician tested
• dermatologist tested
• no quaternium 15

NET WT 4 OZ (113 g)

ZINC OXIDE 
zinc oxide ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 60000-020
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	400 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
PETROLATUM (UNII: 4T6H12BN9U)
COD LIVER OIL (UNII: BBL281NWFG)
LANOLIN (UNII: 7EV65EAW6H)
STARCH, CORN (UNII: O8232NY3SJ)
GLYCERIN (UNII: PDC6A3C0OX)
SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)
YELLOW WAX (UNII: 2ZA36H0S2V)
TOCOPHEROL (UNII: R0ZB2556P8)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 60000-020-12	1 in 1 PACKAGE	07/07/2022	01/12/2023
1		113 g in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	07/07/2022	01/12/2023

Labeler - AHOLD U.S.A., INC. (188910863)

Registrant - Consumer Product Partners, LLC (119091520)

Establishment
Name	Address	ID/FEI	Business Operations
Consumer Product Partners, LLC		119091514	manufacture(60000-020)

Revised: 11/2024

Document Id: 266f6a91-8c42-9a2a-e063-6394a90a6873

34390-5

Set id: 3064f751-5b4e-451c-b5d2-8c132491ef00

Version: 8

Effective Time: 20241108