OTC - ACTIVE INGREDIENT SECTION
Active ingredients Purpose
Salicylic Acid 2% w/w Acne Treatment
Ultra Clear Treatment Lotion
- Manufacturer
- Ultraceuticals Pty Ltd
- Effective date
- 2026-10-07
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 8
- Source
- daily-update
- Hydrated at
- 2026-10-13 04:04:25
Label at a glance#
ProductUltra Clear Treatment
Active ingredientSALICYLIC ACID
Label structure8 sections
Label contents#
Full prescribing information#
OTC - PURPOSE SECTION
Uses
For treatment of acne
Helps clear acne blemishes and acne pimples
INDICATIONS & USAGE SECTION
Stop use and ask a doctor:
If skin irritation becomes severe.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
When using this product
Skin irritation and dryness is more likely to occur if you use another topical acne medication at the same time. If irritation occurs, only use one topical acne medication at a time.
Avoid contact with the eyes. If contact occurs, rinse eyes thoroughly with water to remove.
WARNINGS SECTION
Warnings
For external use only.
When using this product
Skin irritation and dryness is more likely to occur if you use another topical acne medication at the same time. If irritation occurs, only use one topical acne medication at a time.
Avoid contact with the eyes. If contact occurs, rinse eyes thoroughly with water to remove.
DOSAGE & ADMINISTRATION SECTION
Directions
- Clean the skin thoroughly before applying this product. Cover the entire affected area with a thin layer one to three times daily.
- Because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by a doctor.
- If dryness or peeling occurs, reduce application to once a day or every other day.
- If going outside, apply sunscreen after using this product. If irritation or sensitivity develops, stop use of both products and ask a doctor.
INACTIVE INGREDIENT SECTION
Inactive ingredients
Water/Eau, PPG-15 Stearyl Ether, Arginine, Glycerin, Mandelic Acid, Niacinamide, Tribehenin PEG-20 Esters, Ethoxydiglycol, Methylpropanediol, Cetearyl Alcohol, Disodium Laurimodipropionate Tocopheryl Phosphates, Dimethicone, Bentonite, Caprylyl Glycol, Allantoin, Bisabolol, Hydrated Silica, Sodium PCA, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Polyacrylate Crosspolymer-6 Xanthan Gum, Disodium EDTA, Phenylpropanol, Eucalyptus Globulus Leaf Oil, Fusanus Spicata Wood Oil, Phenoxyethanol, Eugenia Caryophyllus (Clove) Bud Oil, Aloe Barbadensis Leaf Juice Powder, Maltodextrin, T-Butyl Alcohol, Benzoic Acid, Dehydroacetic Acid.
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
Ultraceuticals
Ultra Clear Treatment Lotion
with Salicylic & Mandelic Acid
Acne Treatment Lotion
50mL / 1.69 fl OZ
Product Linked Resources#
| Resource | Code type | Value | Equivalent identifiers | Source image |
|---|---|---|---|---|
| Barcode | EAN-13 | 9352207000699 | GTIN-13: 9352207000699 EAN-13: 9352207000699 GTIN storage (14 digits): 09352207000699 | Clear Treatment Carton .jpg |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| 777d68c6-a5ab-e06c-d314-677b0b9af0c8 | Product name | 2 | 20240508 |
| c6f86816-7da6-43ea-8c25-ac9758311cc5 | Product name | 1 | 20220118 |
| 252e11b6-1a9a-4283-a242-df2c129c496d | Product name | 3 | 20170717 |
| 0ca1d589-929b-4b33-bc5b-1d84abdafa6a | Product name | 1 | 20150324 |
| fc363c46-397b-4476-ac0f-70e43e8e4592 | Product name | 1 | 20150324 |
| 1681bc73-b05f-12c3-1075-382ae39f449c | Product name | 1 | 20140508 |
FDA-Initiated Inactive NDC Indexing#
Products#
Every source-derived product name is available through these pages.
- Ultra Clear Treatment
- Salicylic Acid
- LEVOMENOL
- HYDRATED SILICA
- XANTHAN GUM
- DISODIUM LAURIMINODIPROPIONATE TOCOPHERYL PHOSPHATES
- BENTONITE
- SANTALUM SPICATUM OIL
- WATER
- CLOVE OIL
- ALOE VERA LEAF
- TERT-BUTYL ALCOHOL
- BENZOIC ACID
- DEHYDROACETIC ACID
- PPG-15 STEARYL ETHER
- ARGININE
- GLYCERIN
- NIACINAMIDE
- TRIBEHENIN PEG-20 ESTERS
- ALLANTOIN
- PHENOXYETHANOL
- MALTODEXTRIN
- METHYLPROPANEDIOL
- CETOSTEARYL ALCOHOL
- DIMETHICONE
- CAPRYLYL GLYCOL
- AMMONIUM ACRYLOYLDIMETHYLTAURATE, DIMETHYLACRYLAMIDE, LAURYL METHACRYLATE AND LAURETH-4 METHACRYLATE COPOLYMER, TRIMETHYLOLPROPANE TRIACRYLATE CROSSLINKED (45000 MPA.S)
- EDETATE DISODIUM
- EDETIC ACID
- PHENYLPROPANOL
- MANDELIC ACID
- DIETHYLENE GLYCOL MONOETHYL ETHER
- SODIUM PYRROLIDONE CARBOXYLATE
- PYRROLIDONE CARBOXYLIC ACID
- EUCALYPTUS OIL
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 10028-051 | 10028-051-01, 10028-051-02 |
Ingredients#
Every source-derived ingredient row is available through these pages.
Source Document#
Older Hydrated Versions#
| Version | Effective date | Source | Hydrated |
|---|---|---|---|
| 7 | 2025-10-07 | full-release | 2026-06-01 01:38:10 |
| 6 | 2024-10-23 | full-release | 2026-06-01 00:29:08 |
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| 40954e8b-253c-052d-e063-6294a90ad812 | 99b18387-4ab9-4975-e053-2995a90ad6c4 | 2025-10-07 | Warnings | 99b18387-4ab9-4975-e053-2995a90ad6c4 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.