Indications and uses
for the management of acne dries and clears acne blemishes, acne pimples, blackheads, and allows skin to heal helps prevent the development of new acne blemishes, acne pimples and blackheads
Game Over Acne Drying Treatment
- Manufacturer
- Offspring Beauty Co. | KDC/One Chatsworth, Inc.
- Effective date
- 2024-01-09
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 4
- Source
- full-release
- Hydrated at
- 2026-06-01 00:06:56
Label at a glance#
ProductGame Over Acne Drying Treatment
Active ingredientSulfur
Label structure9 sections
Dosage and administration
clean 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 bothersome dryness or peeling occurs, reduce application to once a day or every other day Sensitivity Test for a New U...
Label contents#
Full prescribing information#
SPL UNCLASSIFIED SECTION
Drug Facts
Active ingredient
Sulfur 10%
Purpose
Acne treatment
Uses
- for the management of acne
- dries and clears acne blemishes, acne pimples, blackheads, and allows skin to heal
- helps prevent the development of new acne blemishes, acne pimples and blackheads
Warnings
For external use only.
OTC - WHEN USING 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.
- apply only to areas with acne.
OTC - DO NOT USE SECTION
Do not use on
- broken skin
- large areas of the skin.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Directions
- clean 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 bothersome dryness or peeling occurs, reduce application to once a day or every other day
- Sensitivity Test for a New User: Apply product sparingly to one or two small affected areas during first 3 days. If no discomfort occurs, follow directions above.
Inactive ingredients
Water/Aqua/Eau, Kaolin, Propanediol, Bentonite, Silica, Tetrahexyldecyl Ascorbate, Pentylene Glycol, Butylene Glycol, Phenoxyethanol, Glycerin, Polyacrylate Crosspolymer-6, Ammonium Acryloyldimethyltaurate/VP Copolymer, Sodium Acrylates Copolymer, Dipotassium Glycyrrhizate, Hydrogenated Polyisobutene, Zinc Oxide (CI 77947), Ceramide NP, Citric Acid, Phospholipids, Polyglyceryl-10 Stearate, Sodium Benzotriazolyl Butylphenol Sulfonate, Helianthus Annuus (Sunflower) Seed Oil, Ethylhexylglycerin, Hydroxyphenyl Propamidobenzoic Acid, Tetrasodium Glutamate Diacetate, Terminalia Ferdinandiana Fruit Extract, t-Butyl Alcohol, Podocarpus Elatus Fruit Extract, Pleiogynium Timoriense Fruit Extract, Ascorbyl Palmitate, Sodium Hydroxide, Tocopherol, Sodium Glycolate, Sodium Formate.
SPL UNCLASSIFIED SECTION
Dist. by Offspring Beauty Co.
West Hollywood, CA 90069
PRINCIPAL DISPLAY PANEL - 15 ml Tube Carton
10% SULFUR
ACNE TREATMENT
VERSED
GAME OVER
ACNE DRYING TREATMENT
bentonite + kaolin clay
0.5 fl. oz. | 15 ml
DailyMed RxNorm Mappings#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 73690-026-01 | Game Over Acne Drying Treatment | 1 in 1 CARTON | CREAM | 1 | 4 | |
| 73690-026-01 | Game Over Acne Drying Treatment | 15 mL in 1 TUBE, WITH APPLICATOR | CREAM | 15 | 4 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- Game Over Acne Drying Treatment
- Sulfur
- WATER
- KAOLIN
- PROPANEDIOL
- BENTONITE
- SILICON DIOXIDE
- TETRAHEXYLDECYL ASCORBATE
- PENTYLENE GLYCOL
- BUTYLENE GLYCOL
- PHENOXYETHANOL
- GLYCERIN
- AMMONIUM ACRYLOYLDIMETHYLTAURATE, DIMETHYLACRYLAMIDE, LAURYL METHACRYLATE AND LAURETH-4 METHACRYLATE COPOLYMER, TRIMETHYLOLPROPANE TRIACRYLATE CROSSLINKED (45000 MPA.S)
- AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER
- SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYLTAURATE COPOLYMER (4000000 MW)
- GLYCYRRHIZINATE DIPOTASSIUM
- HYDROGENATED POLYBUTENE (1300 MW)
- CERAMIDE NP
- CITRIC ACID MONOHYDRATE
- LECITHIN, SOYBEAN
- POLYGLYCERYL-10 STEARATE
- SODIUM BENZOTRIAZOLYL BUTYLPHENOL SULFONATE
- SUNFLOWER OIL
- ETHYLHEXYLGLYCERIN
- HYDROXYPHENYL PROPAMIDOBENZOIC ACID
- TETRASODIUM GLUTAMATE DIACETATE
- KAKADU PLUM
- PODOCARPUS ELATUS FRUIT
- PLEIOGYNIUM TIMORIENSE FRUIT
- ZINC OXIDE
- TERT-BUTYL ALCOHOL
- ASCORBYL PALMITATE
- SODIUM HYDROXIDE
- TOCOPHEROL
- SODIUM GLYCOLATE
- SODIUM FORMATE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 73690-026 | 73690-026-01 |
Ingredients#
Every source-derived ingredient row is available through these pages.
Source Document#
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 |
|---|---|---|---|---|---|---|
| 945db8b7-c7fb-4b26-835a-9fb9ab3d2f8c | dfff2d54-d0da-483f-9d40-60f25c108556 | 2024-01-09 | Warnings | 945db8b7-c7fb-4b26-835a-9fb9ab3d2f8c dfff2d54-d0da-483f-9d40-60f25c108556 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.