Baby Oilogic Skin + Aid Diaper Rash Spray

Baby Oilogic Skin Aid Diaper Rash by

Drug Labeling and Warnings

Baby Oilogic Skin Aid Diaper Rash by is a Otc medication manufactured, distributed, or labeled by Ignite Brands, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

BABY OILOGIC SKIN AID DIAPER RASH- zinc oxide spray 
Ignite Brands, LLC

----------

Baby Oilogic Skin + Aid Diaper Rash Spray

Drug Facts

Active ingredient

Zinc Oxide 15%

Purpose

Skin Protectant

Use(s)

• Helps treat and prevent diaper rash
• Protects minor skin irritation associated with diaper rash
• Helps seal out wetness

Warnings

For external use only.

When using this product

• avoid contact with eyes

Stop use and ask a doctor if

• condition lasts more than 7 days or clears up and occurs again within a few days.

Keep out of reach of children.

• If swallowed get medical help or contact a Poison Control Center right away.
• Lock sprayer when not in use.

Directions

• Shake well and unlock before each use.
• Change wet and soiled diapers promptly, cleanse the diaper area, and allow to dry.
• Spray product liberally as often as necessary with each diaper change, especially at bedtime or anytime when exposure to wet diapers may be prolonged.
• Lock sprayer after use.

Inactive Ingredients:

Acacia Senegal Gum, Calendula Officinalis Flower Extract, Caprylhydroxamic Acid, Caprylic/Capric Triglyceride, Caprylyl Glycol, Cellulose Gum, Coco-Caprylate/Caprate, Cocos Nucifera (Coconut) Oil, Glycerin, Lavandula Angustifolia (Lavender) Oil, Methyl Dihydroabietate, Microcrystalline Cellulose, Propanediol, Simmondsia Chinensis (Jojoba) Seed Oil, Tricaprylin, Water (Aqua), Xanthan Gum, Zinc Carbonate.

Other Information

• Store between 59-87° F

Questions?

1-888-645-6442 or www.oilogicbaby.com

package Labeling:

BABY OILOGIC SKIN AID DIAPER RASH 
zinc oxide spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79948-057
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37)	ZINC CATION	150 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ACACIA (UNII: 5C5403N26O)
CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311)
COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H)
COCONUT OIL (UNII: Q9L0O73W7L)
GLYCERIN (UNII: PDC6A3C0OX)
LAVENDER OIL (UNII: ZBP1YXW0H8)
METHYL DIHYDROABIETATE (UNII: 7666FJ0J9F)
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
PROPANEDIOL (UNII: 5965N8W85T)
JOJOBA OIL (UNII: 724GKU717M)
TRICAPRILIN (UNII: 6P92858988)
WATER (UNII: 059QF0KO0R)
XANTHAN GUM (UNII: TTV12P4NEE)
ZINC CARBONATE (UNII: EQR32Y7H0M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79948-057-00	1 in 1 CARTON	06/01/2024	09/04/2025
1		50.3 mL in 1 BOTTLE, SPRAY; 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	06/01/2024	09/04/2025

Labeler - Ignite Brands, LLC (079843577)

Revised: 9/2025

Document Id: 3f01bd84-6024-d001-e063-6394a90a7b8b

34390-5

Set id: 6cc856e5-9ddd-455b-9a28-972755ff2942

Version: 2

Effective Time: 20250917