OTC - ACTIVE INGREDIENT SECTION
Active Ingredients Purpose
Camphor (5%) External Analgesic
Menthol (5%) External Analgesic
Active Ingredients Purpose
Camphor (5%) External Analgesic
Menthol (5%) External Analgesic
Uses:
for the temporary relief of minor aches and pains of muscles and joints due to:
* simple backache * arthritis * sprains * strains * bruises
Warnings:
* for external use only * do not apply to wounds or damaged skin or bandage tightly * avoid contact with eyes * Keep out of reach of children. if swallowed, get medical help or contact a Poison Control Center immediately * if condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days, discontinue use of this product and consult a physician * Pregnancy-breast feeding warning: if pregnant or breast feeding, ask a health professional before use * do not bandage tightly
Inactive Ingredients:
distilled water, hamamelis virginiana (witch hazel extract),
isopropyl alcohol, arnica Montana, oleyl alcohol and
zanthoxylum alatum (scezhuan pepper), Bio-saccharide
Gum -1, glycerin, ammonium acryloyldimethyltaurate/VP
copolymer, beta cyclodextrin, menthol, potassium hydroxide,
mannitol, cellulose chromium, hydroxide green, tocopheryl
acetate (vitamin E), hydroxypropyl methycellulose
Directions:
for adults and children 2 years and older; apply to affected area not more than 3 to 4 times daily. "Children under 2 years of age: consult a doctor." Apply generously to affected and surrounding areas. Rub in well. Use 1 application for minor pain, 2 for medium and 3 applications for severs symptoms. Allow to dry between applications (usually just 2-3 minutes).
Directions:
for adults and children 2 years and older; apply to affected area not more than 3 to 4 times daily. "Children under 2 years of age: consult a doctor." Apply generously to affected and surrounding areas. Rub in well. Use 1 application for minor pain, 2 for medium and 3 applications for severs symptoms. Allow to dry between applications (usually just 2-3 minutes).
Uses:
for the temporary relief of minor aches and pains of muscles
and joints due to:
* simple backache
* arthritis
* sprains
* strains
* bruises
Warnings:
* for external use only
* do not apply to wounds or damaged skin or bandage tightly
* avoid contact with eyes
* Keep out of reach of children. if swallowed, get medical help or contact a Poison Control Center immediately
* if condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days, discontinue use of this product and consult a physician
* Pregnancy-breast feeding warning: if pregnant or breast feeding, ask a health professional before use
* do not bandage tightly
An image/jpeg of the container label is included in this section.
ID: MM1
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 10842-102-01 | 2024-01-30 | C162847 | 48780-1 | 1030e365-5df2-111a-e063-dadaa90a10e2 | Pain Relief Gel |
| 10842-102-02 | 2024-01-30 | C162847 | 48780-1 | 1030e365-5df2-111a-e063-dadaa90a10e2 | Pain Relief Gel |
| 10842-102-03 | 2024-01-30 | C162847 | 48780-1 | 1030e365-5df2-111a-e063-dadaa90a10e2 | Pain Relief Gel |
| 10842-102-04 | 2024-01-30 | C162847 | 48780-1 | 1030e365-5df2-111a-e063-dadaa90a10e2 | Pain Relief Gel |
| 10842-102-05 | 2024-01-30 | C162847 | 48780-1 | 1030e365-5df2-111a-e063-dadaa90a10e2 | Pain Relief Gel |
| 10842-102-08 | 2024-01-30 | C162847 | 48780-1 | 1030e365-5df2-111a-e063-dadaa90a10e2 | Pain Relief Gel |
| 10842-102-09 | 2024-01-30 | C162847 | 48780-1 | 1030e365-5df2-111a-e063-dadaa90a10e2 | Pain Relief Gel |
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 10842-102-01 | Doctor Hoys Natural Pain Relief | 237 mL in 1 BOTTLE, DISPENSING | GEL | 237 | 19 | |
| 10842-102-02 | Doctor Hoys Natural Pain Relief | 1814 mL in 1 JUG | GEL | 1814 | 19 | |
| 10842-102-03 | Doctor Hoys Natural Pain Relief | 118 mL in 1 TUBE | GEL | 118 | 19 | |
| 10842-102-04 | Doctor Hoys Natural Pain Relief | 5 mL in 1 PACKET | GEL | 5 | 19 | |
| 10842-102-05 | Doctor Hoys Natural Pain Relief | 946 mL in 1 JUG | GEL | 946 | 19 | |
| 10842-102-08 | Doctor Hoys Natural Pain Relief | 89 mL in 1 BOTTLE, WITH APPLICATOR | GEL | 89 | 19 | |
| 10842-102-09 | Doctor Hoys Natural Pain Relief | 3785 mL in 1 JUG | GEL | 3785 | 19 |
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| CAMPHOR (NATURAL) | ACTIVE INGREDIENT | N20HL7Q941 | 6 | |
| MENTHOL | ACTIVE INGREDIENT | L7T10EIP3A | 6 | |
| CAMPHOR (NATURAL) | ACTIVE MOIETY | N20HL7Q941 | 6 | |
| MENTHOL | ACTIVE MOIETY | L7T10EIP3A | 6 | |
| ARNICA MONTANA | INACTIVE INGREDIENT | O80TY208ZW | 6 | |
| ISOPROPYL ALCOHOL | INACTIVE INGREDIENT | ND2M416302 | 6 | |
| WATER | INACTIVE INGREDIENT | 059QF0KO0R | 6 | |
| WITCH HAZEL | INACTIVE INGREDIENT | 101I4J0U34 | 6 |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 10842-102 | 10842-102-01, 10842-102-02, 10842-102-04, 10842-102-05, 10842-102-08, 10842-102-09, 10842-102-03 |
Every source-derived ingredient row is available through these pages.
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 |
|---|---|---|---|---|---|---|
| ISOPROPYL ALCOHOL | ISOPROPYL ALCOHOL | ND2M416302 | GEL / TOPICAL | 75 mg | ||
| ISOPROPYL ALCOHOL | ISOPROPYL ALCOHOL | ND2M416302 | SPONGE / TOPICAL | 4 %w/w | ||
| ISOPROPYL ALCOHOL | ISOPROPYL ALCOHOL | ND2M416302 | GEL, METERED / TOPICAL | 525 mg | ||
| ISOPROPYL ALCOHOL | ISOPROPYL ALCOHOL | ND2M416302 | OIL / AURICULAR (OTIC) | 6 mg | ||
| ISOPROPYL ALCOHOL | ISOPROPYL ALCOHOL | ND2M416302 | LOTION, AUGMENTED / TOPICAL | 2070 mg | ||
| ISOPROPYL ALCOHOL | ISOPROPYL ALCOHOL | ND2M416302 | OIL / TOPICAL | 72 mg | ||
| ISOPROPYL ALCOHOL | ISOPROPYL ALCOHOL | ND2M416302 | SOLUTION / TOPICAL | 40 %w/v | ||
| ISOPROPYL ALCOHOL | ISOPROPYL ALCOHOL | ND2M416302 | TABLET, EXTENDED RELEASE / ORAL | NA | ||
| ISOPROPYL ALCOHOL | ISOPROPYL ALCOHOL | ND2M416302 | SWAB / TOPICAL | 43.9 %w/w |
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 |
|---|---|---|---|---|---|---|
| ef195bfa-447b-e58b-e053-2a95a90a7073 | 898f7784-693f-46f6-a9ac-778e0e6aa3b6 | 2022-12-05 | Warnings | ef195bfa-447b-e58b-e053-2a95a90a7073 898f7784-693f-46f6-a9ac-778e0e6aa3b6 |
Adverse event summaries are temporarily unavailable. Other product information remains available.