OTC - ACTIVE INGREDIENT SECTION
Purifying Cleanser
Active ingredient Purpose
Benzoyl Peroxide 2.5%..............Acne Treatment
Active ingredient Purpose
Benzoyl Peroxide 2.5%..............Acne Treatment
BENZOYL PEROXIDE
- Manufacturer
- Wal-Mart Stores Inc | Pharma Pac, LLC
- Effective date
- 2011-02-04
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 10
- Source
- full-release
- Hydrated at
- 2026-05-31 22:27:23
Label at a glance#
ProductBENZOYL PEROXIDE
Active ingredientBENZOYL PEROXIDE
Label structure15 sections
Label contents#
Full prescribing information#
OTC - PURPOSE SECTION
Purifying Cleanser
Active ingredient Purpose
Benzoyl Peroxide 2.5%..............Acne Treatment
Use for the management of acne
Active ingredient Purpose
Benzoyl Peroxide 2.5%..............Acne Treatment
Use for the management of acne
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
Purifying Cleanser Warning Section
Warnings
For external use only
Do not use this medication if you have very sensitive
skin or if you are very sensitive to benzoyl peroxide.
Ask a doctor or pharmacist before use if you are
using other topical acne medications at the same
time or immediately following use of this product.
This may increase dryness or irritation of the skin.
If this occurs, only one medication should be used
unless directed by a doctor.
When using this product
- avoid contact with the eyes. If contact occurs,
rinse eyes thoroughly with water.
- keep away from lips and mouth
- aviod unnecessary sun exposure and use a
sunscreen
Stop use and ask a doctor if skin irritation occurs.
Keep out of the reach of children. If swallowed, get
medical help or contact a Poison Control Center right
away.
Warnings
For external use only
Do not use this medication if you have very sensitive
skin or if you are very sensitive to benzoyl peroxide.
Ask a doctor or pharmacist before use if you are
using other topical acne medications at the same
time or immediately following use of this product.
This may increase dryness or irritation of the skin.
If this occurs, only one medication should be used
unless directed by a doctor.
When using this product
- avoid contact with the eyes. If contact occurs,
rinse eyes thoroughly with water.
- keep away from lips and mouth
- aviod unnecessary sun exposure and use a
sunscreen
Stop use and ask a doctor if skin irritation occurs.
Keep out of the reach of children. If swallowed, get
medical help or contact a Poison Control Center right
away.
INDICATIONS & USAGE SECTION
Purifying Cleanser Directions Section
Directions
- Use morning and night. Apply a small (dime sized)
amount to dampened skin and gently massage for
1 to 2 minutes.
- Rinse thoroughly with warm water
- Pat dry
- If bothersome dryness or peeling occurs, reduce
application to once a day or every other day
- If going outside, use a sunscreen
Other information
- This product may bleach hair or dyed fabrics- Avoid storing at extreme temperatures (below 40
degrees F and above 100 degrees F)
WARNINGS SECTION
Purifying Cleanser Warning Section
Warnings
For external use only
Do not use this medication if you have very sensitive
skin or if you are very sensitive to benzoyl peroxide.
Ask a doctor or pharmacist before use if you are
using other topical acne medications at the same
time or immediately following use of this product.
This may increase dryness or irritation of the skin.
If this occurs, only one medication should be used
unless directed by a doctor.
When using this product
- avoid contact with the eyes. If contact occurs,
rinse eyes thoroughly with water.
- keep away from lips and mouth
- aviod unnecessary sun exposure and use a
sunscreen
Stop use and ask a doctor if skin irritation occurs.
Keep out of the reach of children. If swallowed, get
medical help or contact a Poison Control Center right
away.
Warnings
For external use only
Do not use this medication if you have very sensitive
skin or if you are very sensitive to benzoyl peroxide.
Ask a doctor or pharmacist before use if you are
using other topical acne medications at the same
time or immediately following use of this product.
This may increase dryness or irritation of the skin.
If this occurs, only one medication should be used
unless directed by a doctor.
When using this product
- avoid contact with the eyes. If contact occurs,
rinse eyes thoroughly with water.
- keep away from lips and mouth
- aviod unnecessary sun exposure and use a
sunscreen
Stop use and ask a doctor if skin irritation occurs.
Keep out of the reach of children. If swallowed, get
medical help or contact a Poison Control Center right
away.
DOSAGE & ADMINISTRATION SECTION
Purifying Cleanser Directions Section
Directions
- Use morning and night. Apply a small (dime sized)
amount to dampened skin and gently massage for
1 to 2 minutes.
- Rinse thoroughly with warm water
- Pat dry
- If bothersome dryness or peeling occurs, reduce
application to once a day or every other day
- If going outside, use a sunscreen
Other information
- This product may bleach hair or dyed fabrics- Avoid storing at extreme temperatures (below 40
degrees F and above 100 degrees F)
INACTIVE INGREDIENT SECTION
Purifying Cleanser inactive ingredients section
Inactive Ingredients
purified water, disodium PEG-12 dimethicone
sulfosuccinate, magnesium aluminum silicate,
gyyceryl stearate, tridecyl stearate, neopentyl
glycol dicaprylate/dicaprate, tridecyl trimelliate,
PEG-100 Stearate, sorbitol, dimethyl isosorbide,
polyethylene, cetyl esters, anthemis nobilis flower
extract, xanthan gum, propylene glycol,
imidazolidinyl urea, sodium hyaluronate, sodium
PCA, methylparaben, propylparaben, fragrance
Inactive Ingredients
purified water, disodium PEG-12 dimethicone
sulfosuccinate, magnesium aluminum silicate,
gyyceryl stearate, tridecyl stearate, neopentyl
glycol dicaprylate/dicaprate, tridecyl trimelliate,
PEG-100 Stearate, sorbitol, dimethyl isosorbide,
polyethylene, cetyl esters, anthemis nobilis flower
extract, xanthan gum, propylene glycol,
imidazolidinyl urea, sodium hyaluronate, sodium
PCA, methylparaben, propylparaben, fragrance
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
OTC - ACTIVE INGREDIENT SECTION
Repairing Lotion
Active ingredient Purpose
Benzoyl Peroxide 2.5%..............Acne Treatment
OTC - PURPOSE SECTION
Repairing Lotion
Active ingredient Purpose
Benzoyl Peroxide 2.5%..............Acne Treatment
Use for the management of acne
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
Repairing Lotion Warning Section
Warnings
For external use only
Do not use this medication if you have very sensitive
skin or if you are very sensitive to benzoyl peroxide.
Ask a doctor or pharmacist before use if you are
using other topical acne medications at the same
time or immediately following use of this product.
This may increase dryness or irritation of the skin.
If this occurs, only one medication should be used
unless directed by a doctor.
When using this product
- avoid contact with the eyes. If contact occurs,
rinse eyes thoroughly with water.
- keep away from lips and mouth
- aviod unnecessary sun exposure and use a
sunscreen
Stop use and ask a doctor if skin irritation occurs.
Keep out of the reach of children. If swallowed, get
medical help or contact a Poison Control Center right
away.
Warnings
For external use only
Do not use this medication if you have very sensitive
skin or if you are very sensitive to benzoyl peroxide.
Ask a doctor or pharmacist before use if you are
using other topical acne medications at the same
time or immediately following use of this product.
This may increase dryness or irritation of the skin.
If this occurs, only one medication should be used
unless directed by a doctor.
When using this product
- avoid contact with the eyes. If contact occurs,
rinse eyes thoroughly with water.
- keep away from lips and mouth
- aviod unnecessary sun exposure and use a
sunscreen
Stop use and ask a doctor if skin irritation occurs.
Keep out of the reach of children. If swallowed, get
medical help or contact a Poison Control Center right
away.
INDICATIONS & USAGE SECTION
Repairing Lotion Directions Section
Directions
- Cleanse the skin thoroughly before applyingmedication
- Cover the entire affected area with a thin layer 1 to
3 times daily
- Because excessive drying of the skin may occur,
start with 1 application daily, then gradually
increase to 2 or 3 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
- If going outside, use a sunscreen
Other information
- This product may bleach hair or dyed fabrics
- Avoid storing at extreme temperatures
(below 40 degrees F and above 100 degrees F)
WARNINGS SECTION
Repairing Lotion Warning Section
Warnings
For external use only
Do not use this medication if you have very sensitive
skin or if you are very sensitive to benzoyl peroxide.
Ask a doctor or pharmacist before use if you are
using other topical acne medications at the same
time or immediately following use of this product.
This may increase dryness or irritation of the skin.
If this occurs, only one medication should be used
unless directed by a doctor.
When using this product
- avoid contact with the eyes. If contact occurs,
rinse eyes thoroughly with water.
- keep away from lips and mouth
- aviod unnecessary sun exposure and use a
sunscreen
Stop use and ask a doctor if skin irritation occurs.
Keep out of the reach of children. If swallowed, get
medical help or contact a Poison Control Center right
away.
Warnings
For external use only
Do not use this medication if you have very sensitive
skin or if you are very sensitive to benzoyl peroxide.
Ask a doctor or pharmacist before use if you are
using other topical acne medications at the same
time or immediately following use of this product.
This may increase dryness or irritation of the skin.
If this occurs, only one medication should be used
unless directed by a doctor.
When using this product
- avoid contact with the eyes. If contact occurs,
rinse eyes thoroughly with water.
- keep away from lips and mouth
- aviod unnecessary sun exposure and use a
sunscreen
Stop use and ask a doctor if skin irritation occurs.
Keep out of the reach of children. If swallowed, get
medical help or contact a Poison Control Center right
away.
DOSAGE & ADMINISTRATION SECTION
Repairing Lotion Directions Section
Directions
- Cleanse the skin thoroughly before applyingmedication
- Cover the entire affected area with a thin layer 1 to
3 times daily
- Because excessive drying of the skin may occur,
start with 1 application daily, then gradually
increase to 2 or 3 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
- If going outside, use a sunscreen
Other information
- This product may bleach hair or dyed fabrics
- Avoid storing at extreme temperatures
(below 40 degrees F and above 100 degrees F)
INACTIVE INGREDIENT SECTION
Repairing Lotion inactive ingredients section
Inactive ingredients
purified water, cetearyl alcohol, ceteareth-20,
ethoxydiglycol, cyclotetrasiloxane, propylene
glycol, dimethicone, glyceryl stearate,
cyclopentasiloxane diazolidinyl urea, methylparaben,
propylparaben, PEG-100 stearate, panthenol,
allantoin, triethanolamine, carbomer, fragrance,
xanthan gum
Inactive ingredients
purified water, cetearyl alcohol, ceteareth-20,
ethoxydiglycol, cyclotetrasiloxane, propylene
glycol, dimethicone, glyceryl stearate,
cyclopentasiloxane diazolidinyl urea, methylparaben,
propylparaben, PEG-100 stearate, panthenol,
allantoin, triethanolamine, carbomer, fragrance,
xanthan gum
DailyMed RxNorm Mappings#
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| a46239a7-5963-4008-8cbb-6b9000f497eb | Product name | 1 | 20250721 |
| b382b4e1-6b48-45f6-bffc-e61b00b0ce19 | Product name | 3 | 20250317 |
| d9d61457-6a5a-41fc-b418-e5479a2904b7 | Product name | 2 | 20230303 |
| 32012d5c-25ac-49c7-9d4c-1313177fff7c | Product name | 1 | 20230112 |
| 13e7e7e3-e885-4c79-af6d-dad1aedbb06e | Product name | 1 | 20220128 |
| 4a7d44fe-774d-404b-aad0-8a90fe78375a | Product name | 4 | 20211025 |
| 3f45980c-c196-47e5-0e5e-48b7c57327c5 | Product name | 5 | 20200428 |
| d12e2d7c-bd6b-45d4-94f9-6df8e1b8b27b | Product name | 3 | 20200203 |
| ee5c6de5-d9cd-454f-b250-7b19e5cf2992 | Product name | 4 | 20190619 |
| ad75fcfd-a339-42a1-9c60-43ba2c654cfa | Product name | 1 | 20170810 |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 49035-021-13 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-89a1-f424-e053-dadaa90a57ce | drug facts |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 49035-021-13 | BENZOYL PEROXIDE | 1 in 1 KIT | KIT | 1 | 10 |
DailyMed Dashboard NDC Coverage#
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| BENZOYL PEROXIDE | ACTIVE INGREDIENT | W9WZN9A0GM | 10 | |
| BENZOYL PEROXIDE | ACTIVE MOIETY | W9WZN9A0GM | 10 | |
| ALLANTOIN | INACTIVE INGREDIENT | 344S277G0Z | 10 | |
| CARBOMER HOMOPOLYMER TYPE C | INACTIVE INGREDIENT | 4Q93RCW27E | 10 | |
| CETOSTEARYL ALCOHOL | INACTIVE INGREDIENT | 2DMT128M1S | 10 | |
| CETYL ESTERS WAX | INACTIVE INGREDIENT | D072FFP9GU | 10 | |
| CHAMAEMELUM NOBILE FLOWER | INACTIVE INGREDIENT | O2T154T6OG | 10 | |
| DIAZOLIDINYL UREA | INACTIVE INGREDIENT | H5RIZ3MPW4 | 10 | |
| DIETHYLENE GLYCOL MONOETHYL ETHER | INACTIVE INGREDIENT | A1A1I8X02B | 10 | |
| DIMETHICONE | INACTIVE INGREDIENT | 92RU3N3Y1O | 10 | |
| DIMETHYL ISOSORBIDE | INACTIVE INGREDIENT | SA6A6V432S | 10 | |
| GLYCERYL MONOSTEARATE | INACTIVE INGREDIENT | 230OU9XXE4 | 10 | |
| HIGH DENSITY POLYETHYLENE | INACTIVE INGREDIENT | UG00KM4WR7 | 10 | |
| HYALURONATE SODIUM | INACTIVE INGREDIENT | YSE9PPT4TH | 10 | |
| IMIDUREA | INACTIVE INGREDIENT | M629807ATL | 10 | |
| MAGNESIUM ALUMINUM SILICATE | INACTIVE INGREDIENT | 6M3P64V0NC | 10 | |
| METHYLPARABEN | INACTIVE INGREDIENT | A2I8C7HI9T | 10 | |
| NEOPENTYL GLYCOL | INACTIVE INGREDIENT | QI80HXD6S5 | 10 | |
| PANTHENOL | INACTIVE INGREDIENT | WV9CM0O67Z | 10 | |
| PEG-12 STEARATE | INACTIVE INGREDIENT | 9KU38O8CEK | 10 | |
| POLYOXYL 100 STEARATE | INACTIVE INGREDIENT | YD01N1999R | 10 | |
| POLYOXYL 20 CETOSTEARYL ETHER | INACTIVE INGREDIENT | YRC528SWUY | 10 | |
| PROPYLENE GLYCOL | INACTIVE INGREDIENT | 6DC9Q167V3 | 10 | |
| PROPYLPARABEN | INACTIVE INGREDIENT | Z8IX2SC1OH | 10 | |
| SODIUM PYRROLIDONE CARBOXYLATE | INACTIVE INGREDIENT | 469OTG57A2 | 10 | |
| SORBITOL | INACTIVE INGREDIENT | 506T60A25R | 10 | |
| TRIDECYL STEARATE | INACTIVE INGREDIENT | A8OE252M6L | 10 | |
| TROLAMINE | INACTIVE INGREDIENT | 9O3K93S3TK | 10 | |
| Water | INACTIVE INGREDIENT | 059QF0KO0R | 10 | |
| XANTHAN GUM | INACTIVE INGREDIENT | TTV12P4NEE | 10 |
Products#
Every source-derived product name is available through these pages.
- BENZOYL PEROXIDE
- WATER
- MAGNESIUM ALUMINUM SILICATE
- GLYCERYL MONOSTEARATE
- POLYOXYL 100 STEARATE
- PEG-12 STEARATE
- SORBITOL
- DIMETHYL ISOSORBIDE
- TRIDECYL STEARATE
- NEOPENTYL GLYCOL
- HIGH DENSITY POLYETHYLENE
- CETYL ESTERS WAX
- CHAMAEMELUM NOBILE FLOWER
- HYALURONATE SODIUM
- SODIUM PYRROLIDONE CARBOXYLATE
- XANTHAN GUM
- IMIDUREA
- METHYLPARABEN
- PROPYLPARABEN
- DIETHYLENE GLYCOL MONOETHYL ETHER
- POLYOXYL 20 CETOSTEARYL ETHER
- CETOSTEARYL ALCOHOL
- PROPYLENE GLYCOL
- DIMETHICONE
- DIAZOLIDINYL UREA
- PANTHENOL
- ALLANTOIN
- CARBOMER HOMOPOLYMER TYPE C
- TROLAMINE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 49035-021 | 49035-021-13 |
Ingredients#
Every source-derived ingredient row is available through these pages.
Source Document#
Inactive ingredient matches#
Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.
| DailyMed ingredient | IID ingredient | UNII | Dosage form / route | Potency | Maximum daily exposure | Match |
|---|---|---|---|---|---|---|
| CARBOMER HOMOPOLYMER TYPE C | CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) | 4Q93RCW27E | GEL / TRANSDERMAL | 150 mg | ||
| PROPYLENE GLYCOL | PROPYLENE GLYCOL | 6DC9Q167V3 | SUSPENSION/ DROPS / TOPICAL | 0.75 %w/v | ||
| GLYCERYL MONOSTEARATE | GLYCERYL MONOSTEARATE | 230OU9XXE4 | TABLET / ORAL | 33.34 mg | ||
| ALLANTOIN | ALLANTOIN | 344S277G0Z | GEL / TOPICAL | 8 mg | ||
| GLYCERYL MONOSTEARATE | GLYCERYL MONOSTEARATE | 230OU9XXE4 | SUSPENSION / OPHTHALMIC | 0.5 %w/v | ||
| PROPYLPARABEN | PROPYLPARABEN | Z8IX2SC1OH | INJECTION / INTRALESIONAL | 0.02 %w/v | ||
| PROPYLENE GLYCOL | PROPYLENE GLYCOL | 6DC9Q167V3 | TABLET / ORAL | 64 mg | ||
| HIGH DENSITY POLYETHYLENE | HIGH DENSITY POLYETHYLENE | UG00KM4WR7 | CREAM / TOPICAL | 54.5 %w/w | ||
| GLYCERYL MONOSTEARATE | GLYCERYL MONOSTEARATE | 230OU9XXE4 | AEROSOL, FOAM / VAGINAL | 3 %w/w | ||
| HIGH DENSITY POLYETHYLENE | HIGH DENSITY POLYETHYLENE | UG00KM4WR7 | TABLET, COATED / ORAL | 25 mg | ||
| CETOSTEARYL ALCOHOL | CETOSTEARYL ALCOHOL | 2DMT128M1S | AEROSOL, FOAM / TOPICAL | 21 mg | ||
| SORBITOL | SORBITOL | 506T60A25R | ELIXIR / ORAL | 833.3 mg | ||
| MAGNESIUM ALUMINUM SILICATE | MAGNESIUM ALUMINUM SILICATE | 6M3P64V0NC | SHAMPOO / TOPICAL | 1.25 %w/w | ||
| PROPYLPARABEN | PROPYLPARABEN | Z8IX2SC1OH | INJECTION, SOLUTION / INTRAVENOUS | 5 mg | ||
| METHYLPARABEN | METHYLPARABEN | A2I8C7HI9T | SOLUTION / TOPICAL | 216 mg | ||
| PROPYLPARABEN | PROPYLPARABEN | Z8IX2SC1OH | INJECTION / INFILTRATION | 0.35 mg | ||
| PROPYLPARABEN | PROPYLPARABEN | Z8IX2SC1OH | CONCENTRATE / ORAL | 2.5 mg/5ml | ||
| PROPYLPARABEN | PROPYLPARABEN | Z8IX2SC1OH | OINTMENT / OPHTHALMIC | 0.01 %w/w | ||
| PROPYLENE GLYCOL | PROPYLENE GLYCOL | 6DC9Q167V3 | SOLUTION / OPHTHALMIC | 1 %w/v | ||
| PROPYLENE GLYCOL | PROPYLENE GLYCOL | 6DC9Q167V3 | SHAMPOO, SUSPENSION / TOPICAL | 2 %w/w | ||
| PROPYLENE GLYCOL | PROPYLENE GLYCOL | 6DC9Q167V3 | DROPS / ORAL | 200 mg/1ml | ||
| PROPYLENE GLYCOL | PROPYLENE GLYCOL | 6DC9Q167V3 | SPRAY / NASAL | 5 mg | ||
| SORBITOL | SORBITOL | 506T60A25R | INJECTION / INTRAMUSCULAR | NA | ||
| PROPYLPARABEN | PROPYLPARABEN | Z8IX2SC1OH | SOLUTION / RESPIRATORY (INHALATION) | 0.01 %w/w | ||
| DIMETHYL ISOSORBIDE | DIMETHYL ISOSORBIDE | SA6A6V432S | AEROSOL, FOAM / TOPICAL | 5.44 %w/w | ||
| MAGNESIUM ALUMINUM SILICATE | MAGNESIUM ALUMINUM SILICATE | 6M3P64V0NC | POWDER, FOR SUSPENSION / ORAL | NA | ||
| METHYLPARABEN | METHYLPARABEN | A2I8C7HI9T | CREAM / TOPICAL | 3000 mg | ||
| PROPYLPARABEN | PROPYLPARABEN | Z8IX2SC1OH | INJECTION / SUBCUTANEOUS | 2 mg | ||
| PROPYLENE GLYCOL | PROPYLENE GLYCOL | 6DC9Q167V3 | GEL / RECTAL | 3315 mg | ||
| SORBITOL | SORBITOL | 506T60A25R | INJECTION / INTRAVENOUS | 1276 mg | ||
| PROPYLPARABEN | PROPYLPARABEN | Z8IX2SC1OH | SOLUTION, CONCENTRATE / ORAL | 0.2 mg/1ml | ||
| CETYL ESTERS WAX | CETYL ESTERS WAX | D072FFP9GU | POWDER, FOR SUSPENSION / ORAL | NA | ||
| SORBITOL | SORBITOL | 506T60A25R | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION / INTRAVENOUS | 1.04 %w/v | ||
| XANTHAN GUM | XANTHAN GUM | TTV12P4NEE | SUSPENSION / TOPICAL | 0.11 %w/v | ||
| SORBITOL | SORBITOL | 506T60A25R | SUSPENSION / ORAL | 45000 mg | ||
| METHYLPARABEN | METHYLPARABEN | A2I8C7HI9T | ELIXIR / ORAL | 800 mg | ||
| PROPYLENE GLYCOL | PROPYLENE GLYCOL | 6DC9Q167V3 | TABLET, FILM COATED, EXTENDED RELEASE / ORAL | 19 mg | ||
| XANTHAN GUM | XANTHAN GUM | TTV12P4NEE | POWDER, FOR SOLUTION / ORAL | 10 mg/5ml | ||
| PROPYLENE GLYCOL | PROPYLENE GLYCOL | 6DC9Q167V3 | SOLUTION, CONCENTRATE / ORAL | 2590 mg | ||
| METHYLPARABEN | METHYLPARABEN | A2I8C7HI9T | INJECTION / SUBCUTANEOUS | 22 mg | ||
| SORBITOL | SORBITOL | 506T60A25R | POWDER, FOR SUSPENSION / ORAL | 12000 mg | ||
| SORBITOL | SORBITOL | 506T60A25R | INJECTION, SOLUTION / INTRAVENOUS | 4050 mg | ||
| SODIUM PYRROLIDONE CARBOXYLATE | SODIUM PYRROLIDONE CARBOXYLATE | 469OTG57A2 | LOTION / TOPICAL | 42 mg | ||
| SORBITOL | SORBITOL | 506T60A25R | SUSPENSION / RECTAL | 46.18 %w/v | ||
| PROPYLENE GLYCOL | PROPYLENE GLYCOL | 6DC9Q167V3 | SUPPOSITORY / VAGINAL | 252 mg | ||
| HYALURONATE SODIUM | HYALURONATE SODIUM | YSE9PPT4TH | INJECTION, SUSPENSION / INTRA-ARTICULAR | 23 mg | ||
| SORBITOL | SORBITOL | 506T60A25R | INJECTION, SOLUTION / SUBCUTANEOUS | 4.7 %w/v | ||
| PROPYLENE GLYCOL | PROPYLENE GLYCOL | 6DC9Q167V3 | JELLY / TOPICAL | 20 %w/w | ||
| TROLAMINE | TROLAMINE | 9O3K93S3TK | AEROSOL, FOAM / VAGINAL | 2 %w/w | ||
| METHYLPARABEN | METHYLPARABEN | A2I8C7HI9T | SUSPENSION / SUBCUTANEOUS | 0.16 %w/v | ||
| METHYLPARABEN | METHYLPARABEN | A2I8C7HI9T | CAPSULE / ORAL | 7 mg | ||
| METHYLPARABEN | METHYLPARABEN | A2I8C7HI9T | CREAM / VAGINAL | 22 mg | ||
| PROPYLPARABEN | PROPYLPARABEN | Z8IX2SC1OH | INJECTION / INTRA-ARTICULAR | 0.03 %w/v | ||
| XANTHAN GUM | XANTHAN GUM | TTV12P4NEE | CREAM / TOPICAL | 46 mg | ||
| CARBOMER HOMOPOLYMER TYPE C | CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) | 4Q93RCW27E | OINTMENT, AUGMENTED / TOPICAL | 23 mg | ||
| SORBITOL | SORBITOL | 506T60A25R | CREAM / TOPICAL | 36.8 %w/w | ||
| MAGNESIUM ALUMINUM SILICATE | MAGNESIUM ALUMINUM SILICATE | 6M3P64V0NC | SUSPENSION / ORAL | 5000 mg/5ml | ||
| PROPYLPARABEN | PROPYLPARABEN | Z8IX2SC1OH | INJECTION, POWDER, FOR SOLUTION / INTRAVENOUS | 0.8 mg | ||
| METHYLPARABEN | METHYLPARABEN | A2I8C7HI9T | SOLUTION / RECTAL | 0.13 %w/v | ||
| PROPYLPARABEN | PROPYLPARABEN | Z8IX2SC1OH | DROPS / AURICULAR (OTIC) | NA |
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 |
|---|---|---|---|---|---|---|
| 4d9de360-92c8-4d41-bb59-7d62656396dc | bafc44bf-4e1f-4729-a96e-828dc2875486 | 2011-02-04 | Warnings | 4d9de360-92c8-4d41-bb59-7d62656396dc bafc44bf-4e1f-4729-a96e-828dc2875486 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.