Label: AQUAPHOR ITCH RELIEF- hydrocortisone ointment
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NDC Code(s):
10356-120-04,
10356-120-07,
10356-120-30,
10356-120-52, view more10356-120-53, 10356-120-54
- Packager: Beiersdorf Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 31, 2024
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- DO NOT USE
- WHEN USING
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
- INACTIVE INGREDIENT
- QUESTIONS
-
PRINCIPAL DISPLAY PANEL
Aquaphor Itch Relief Ointment
Maximum Strength
Immediately Soothes & Relieves Itch & Irritiation
Up to 12 hours Significant Itch Relief
Clinically Proven
1% Hydrocortisone Anti-Itch Ointment
Dermatologist Recommended Brand
Fragrance free and Paraben free
Hypoallergenic
Helps Heal the Itch
Clinically proven significant itch relief for up to 12 hours
Immediately soothes itchy spots to help skin heal
Skin irritation
Skin rashes
Eczema
Psoriasis
Eczema
Poison Ivy
Children's
Aquaphor Itch Relief Ointment
Ages 2 Years and Older
Immediately Soothes & Relieves Itch & Irritiation
Up to 12 hours Significant Itch Relief
Clinically Proven
Number 1 Pediatrician Recommended Brand for Eczema
1% Hydrocortisone Anti-Itch Ointment
Dermatologist Recommended Brand
Fragrance free and Paraben free
Hypoallergenic
Helps Heal the Itch
Clinically proven significant itch relief for up to 12 hours
Immediately soothes itchy spots to help skin heal
Eczema
Skin irritation
Skin rashes
Psoriasis
Eczema
Poison Ivy
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INGREDIENTS AND APPEARANCE
AQUAPHOR ITCH RELIEF
hydrocortisone ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:10356-120 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HYDROCORTISONE (UNII: WI4X0X7BPJ) (HYDROCORTISONE - UNII:WI4X0X7BPJ) HYDROCORTISONE 1 g in 100 g Inactive Ingredients Ingredient Name Strength 3-((L-MENTHYL)OXY)PROPANE-1,2-DIOL (UNII: KD6TZ2QICH) MINERAL OIL (UNII: T5L8T28FGP) CERESIN (UNII: Q1LS2UJO3A) LANOLIN ALCOHOLS (UNII: 884C3FA9HE) GLYCERIN (UNII: PDC6A3C0OX) PANTHENOL (UNII: WV9CM0O67Z) LEVOMENOL (UNII: 24WE03BX2T) PETROLATUM (UNII: 4T6H12BN9U) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:10356-120-30 0.9 g in 1 PACKET; Type 0: Not a Combination Product 11/01/2020 2 NDC:10356-120-52 1 in 1 CARTON 11/01/2020 2 NDC:10356-120-04 28 g in 1 TUBE; Type 0: Not a Combination Product 3 NDC:10356-120-04 28 g in 1 TUBE; Type 0: Not a Combination Product 11/01/2020 4 NDC:10356-120-53 2 in 1 CARTON 11/01/2020 4 NDC:10356-120-04 28 g in 1 TUBE; Type 0: Not a Combination Product 5 NDC:10356-120-54 1 in 1 CARTON 06/01/2021 5 NDC:10356-120-07 56 g in 1 TUBE; Type 0: Not a Combination Product 6 NDC:10356-120-07 56 g in 1 TUBE; Type 0: Not a Combination Product 06/01/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M017 11/01/2020 Labeler - Beiersdorf Inc (001177906)