Storage and handling
Other Information Do not store above 30 o C or 86 o F.
Botanics Daily Hand Therapy Sunscreen SPF 10
- Manufacturer
- Boots Retail USA Inc | The Boots Company PLC | BCM Ltd
- Effective date
- 2010-02-01
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-05-31 22:23:29
Label at a glance#
ProductBotanics Daily Hand Therapy Sunscreen SPF 10
Active ingredientOctinoxate, Avobenzone
Label structure20 sections
Contacts and useful links#
Websitewww.boots.com
www.boots.com
www.boots.comLabel contents#
Full prescribing information#
OTC - ACTIVE INGREDIENT SECTION
Active Ingredients Purpose
Avobenzone 2% Sunscreens
Octinoxate 4%
OTC - PURPOSE SECTION
Uses
- Provides minimal protection against the adverse effects of the sun
- Higher SPF gives more protection
WARNINGS AND PRECAUTIONS SECTION
Warnings
For external use only
When using this product keep out of eyes. If contact occurs rinse thoroughly with cold water. Avoid direct contact with fabric.
HOW SUPPLIED SECTION
Colour may vary due to natural extracts
OTC - ASK DOCTOR SECTION
Stop use and ask a doctor if rash or irritation develops and lasts.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
Keep out of reach of children. If swallowed, get medical help.
INDICATIONS & USAGE SECTION
Directions
- Massage into hands daily
- Apply evenly at least 15 minutes before sun exposure.
- Reapply as required.
- Not intended for children under the age of 12.
- Not intended for protection while sunbathing.
STORAGE AND HANDLING SECTION
Other Information
Do not store above 30oC or 86oF.
INACTIVE INGREDIENT SECTION
Inactive ingredients
Aqua (Water), C12-15 alkyl benzoate, Butylene glycol, Dimethicone, Cetyl alcohol, Paraffinum liquidum (Mineral oil), Sorbitan stearate, Petrolatum, C18-36 acid glycol ester, Glycerin, Butyrospermum parkii (Shea butter), Phenoxyethanol, Vaccinium myrtillus extract, Carbomer, Methylparaben, Xanthan gum, Parfum (Fragrance), Propylparaben, Potassium hydroxide, Sucrose cocoate, Equisetum arvense extract, Dipropylene glycol, Tetrasodium EDTA, BHT
OTC - QUESTIONS SECTION
USA: Questions? 1-866-75-BOOTS
DESCRIPTION SECTION
EXTRACTS AUTHENTICATED BY ROYAL BOTANIC GARDENS KEW
ACTIVE PLANT EXTRACTS
Plant extracts at levels that really work, combined and formulated for unbeatable product performance.
Naturally.
Hands show the signs of ageing just as much as the face. This light cream helps protect hands from free radical damage and premature skin ageing. Easily absorbed so you can use it all day long, it sinks into skin to plump and moisturise leaving your hands beautifully soft, smooth and supple.
Dermatologically tested.
INFORMATION FOR PATIENTS SECTION
Mfd in the U.K. for BBI NG2 3AA. UK.
Dist in the USA by Boots Retail USA Inc. Stamford CT 06901
USA: Questions? 1-866-75-BOOTS
DESCRIPTION SECTION
Tube label
ACTIVE PLANT EXTRACTS
Plant extract at levels that really work. Naturally.
This light cream helps protect hands from free radical damage and premature skin ageing. Easily absorbed so you can use it all day long.
Dermatologically tested.
EXTRAITS ACTIFS DE PLANTES
Des extraits de plantes à des degrés efficaces. Tout naturellement.
Cette crème légère aide à protéger les main des radicaux libres et lutte contre le vieillissement prematuré. Facilement absorbée, elle peau être utilisée tout au long de la journée.
Dermo-testé
INDICATIONS & USAGE SECTION
DIRECTIONS: Massage into hands daily.
MODE D'EMPLOI: Massage des main au quotidian.
WARNINGS AND PRECAUTIONS SECTION
WARNINGS: Avoid getting directly in eyes. If contact occurs rinse thoroughly with cold water. Avoid direct contact with fabric.
MISE EN GARDE: Éviter tout contact avec les yeux. En cas de projection, rincer immédiatement à l'eau froide. Éviter tout contact direct avec du tissu.
HOW SUPPLIED SECTION
Colour may vary due to natural extracts.
La couleur peut varier en raison des extraits naturels.
OTC - ACTIVE INGREDIENT SECTION
ACTIVE INGREDIENTS/ACTIFS: Octinoxate 4.0% Avobenzone 2.0%.
INFORMATION FOR PATIENTS SECTION
EXTRACTS AUTHENTICATED BY ROYAL BOTANIC GARDENS KEW
EXTRAITS APPROUVES PAR LES JARDINS BOTANIQUES ROYAUX DE KEW
Mfd in the U.K. for/Fabriqué au R.-U. pour BBI NG2 3AA. UK.
Dist in the USA by/aux É.-U. par Boots Retail USA Inc. Stamford CT 06901
USA/Canada: Questions? 1-866-75-BOOTS
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
Carton label
Daily Hand Therapy Sunscreen SPF 10
Bilberry to protect and brighten
Cure Quotidienne Des Main Protection Solaire FPS 10
La myrtille protège et éclaircit
Boots
The Power of Plants
Botanics
75ml e 2.5 US Fl. Oz
Daily Hand Therapy carton.jpg
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
Tube label
Daily Hand Therapy Sunscreen SPF 10
Bilberry to protect and brighten
Cure Quotidienne Des Main Protection Solaire FPS 10
La myrtille protège et éclaircit
Boots
The Power of Plants
Botanics
75ml e 2.5 US Fl. Oz
Daily Hand Therapy label.jpg
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 68472-049-01 | 2019-10-21 | C162847 | 48780-1 | 956f9ecf-c861-621f-e053-dbdaa90a74ad | Carton and tube labelling |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 68472-049-01 | Botanics Daily Hand Therapy Sunscreen SPF 10 | 75 mL in 1 TUBE | CREAM | 75 | 1 | |
| 68472-049-01 | Botanics Daily Hand Therapy Sunscreen SPF 10 | 1 in 1 CARTON | CREAM | 1 | 1 |
DailyMed Dashboard NDC Coverage#
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| Avobenzone | ACTIVE INGREDIENT | G63QQF2NOX | 1 | |
| Octinoxate | ACTIVE INGREDIENT | 4Y5P7MUD51 | 1 | |
| Avobenzone | ACTIVE MOIETY | G63QQF2NOX | 1 | |
| Octinoxate | ACTIVE MOIETY | 4Y5P7MUD51 | 1 | |
| Butylated Hydroxytoluene | INACTIVE INGREDIENT | 1P9D0Z171K | 1 | |
| Butylene Glycol | INACTIVE INGREDIENT | 3XUS85K0RA | 1 | |
| Carbomer Homopolymer Type C | INACTIVE INGREDIENT | 4Q93RCW27E | 1 | |
| Cetyl Alcohol | INACTIVE INGREDIENT | 936JST6JCN | 1 | |
| Dimethicone | INACTIVE INGREDIENT | 92RU3N3Y1O | 1 | |
| Glycerin | INACTIVE INGREDIENT | PDC6A3C0OX | 1 | |
| Methylparaben | INACTIVE INGREDIENT | A2I8C7HI9T | 1 | |
| Mineral Oil | INACTIVE INGREDIENT | T5L8T28FGP | 1 | |
| Petrolatum | INACTIVE INGREDIENT | 4T6H12BN9U | 1 | |
| Phenoxyethanol | INACTIVE INGREDIENT | HIE492ZZ3T | 1 | |
| Potassium Hydroxide | INACTIVE INGREDIENT | WZH3C48M4T | 1 | |
| Propylparaben | INACTIVE INGREDIENT | Z8IX2SC1OH | 1 | |
| Shea Butter | INACTIVE INGREDIENT | K49155WL9Y | 1 | |
| Sorbitan Monostearate | INACTIVE INGREDIENT | NVZ4I0H58X | 1 | |
| Vaccinium Myrtillus Leaf | INACTIVE INGREDIENT | Y4U591OU70 | 1 | |
| Water | INACTIVE INGREDIENT | 059QF0KO0R | 1 | |
| Xanthan Gum | INACTIVE INGREDIENT | TTV12P4NEE | 1 |
Products#
Every source-derived product name is available through these pages.
- Botanics Daily Hand Therapy Sunscreen SPF 10
- Octinoxate and Avobenzone
- Octinoxate
- Avobenzone
- Water
- Butylene Glycol
- Dimethicone
- Cetyl Alcohol
- Mineral Oil
- Sorbitan Monostearate
- Petrolatum
- Glycerin
- Shea Butter
- Phenoxyethanol
- Vaccinium Myrtillus Leaf
- Carbomer Homopolymer Type C
- Methylparaben
- Xanthan Gum
- Propylparaben
- Potassium Hydroxide
- Butylated Hydroxytoluene
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 68472-049 | 68472-049-01 |
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 |
|---|---|---|---|---|---|---|
| Propylparaben | PROPYLPARABEN | Z8IX2SC1OH | SUSPENSION / RECTAL | 271 mg | ||
| Propylparaben | PROPYLPARABEN | Z8IX2SC1OH | LIQUID / ORAL | 2 mg | ||
| Xanthan Gum | XANTHAN GUM | TTV12P4NEE | FILM, SOLUBLE / ORAL | 1 mg | ||
| Phenoxyethanol | PHENOXYETHANOL | HIE492ZZ3T | AEROSOL, FOAM / TOPICAL | 72 mg | ||
| Glycerin | GLYCERIN | PDC6A3C0OX | SUSPENSION/ DROPS / ORAL | 750 mg | ||
| Petrolatum | PETROLATUM | 4T6H12BN9U | SOAP / TOPICAL | 0.85 %w/w | ||
| Glycerin | GLYCERIN | PDC6A3C0OX | SYSTEM / TOPICAL | 18144 mg | ||
| Butylated Hydroxytoluene | BUTYLATED HYDROXYTOLUENE | 1P9D0Z171K | CAPSULE, LIQUID FILLED / ORAL | 0.1 mg | ||
| Glycerin | GLYCERIN | PDC6A3C0OX | JELLY / TOPICAL | NA | ||
| Glycerin | GLYCERIN | PDC6A3C0OX | SOLUTION / OPHTHALMIC | 6 %w/v | ||
| Glycerin | GLYCERIN | PDC6A3C0OX | OINTMENT / TOPICAL | NA | ||
| Cetyl Alcohol | CETYL ALCOHOL | 936JST6JCN | TABLET, FILM COATED / ORAL | NA | ||
| Glycerin | GLYCERIN | PDC6A3C0OX | PASTE, DENTIFRICE / DENTAL | 18 %w/w | ||
| Carbomer Homopolymer Type C | CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) | 4Q93RCW27E | CREAM, AUGMENTED / TOPICAL | 20 mg | ||
| Methylparaben | METHYLPARABEN | A2I8C7HI9T | JELLY / TOPICAL | 420 mg | ||
| Glycerin | GLYCERIN | PDC6A3C0OX | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION / INTRAVENOUS | 225 mg | ||
| Propylparaben | PROPYLPARABEN | Z8IX2SC1OH | SOLUTION / OPHTHALMIC | 0.02 %w/w | ||
| Xanthan Gum | XANTHAN GUM | TTV12P4NEE | GRANULE, FOR SUSPENSION / ORAL | 450 mg | ||
| Methylparaben | METHYLPARABEN | A2I8C7HI9T | FILM, SOLUBLE / BUCCAL | 3 mg | ||
| Petrolatum | PETROLATUM | 4T6H12BN9U | LIQUID / RESPIRATORY (INHALATION) | NA | ||
| Butylated Hydroxytoluene | BUTYLATED HYDROXYTOLUENE | 1P9D0Z171K | LOTION / TOPICAL | 1000 mg | ||
| Propylparaben | PROPYLPARABEN | Z8IX2SC1OH | INJECTION, POWDER, FOR SOLUTION / INTRAMUSCULAR | 0.4 mg | ||
| Methylparaben | METHYLPARABEN | A2I8C7HI9T | INJECTION / INTRALESIONAL | 0.15 %w/v | ||
| Sorbitan Monostearate | SORBITAN MONOSTEARATE | NVZ4I0H58X | LOTION / TOPICAL | 89 mg | ||
| Methylparaben | METHYLPARABEN | A2I8C7HI9T | INJECTION / INTRAVENOUS | 95 mg | ||
| Sorbitan Monostearate | SORBITAN MONOSTEARATE | NVZ4I0H58X | SUSPENSION / TOPICAL | 2.15 %w/w | ||
| Glycerin | GLYCERIN | PDC6A3C0OX | AEROSOL / TOPICAL | 3 %w/w | ||
| Carbomer Homopolymer Type C | CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) | 4Q93RCW27E | GEL, METERED / TRANSDERMAL | 50 mg | ||
| Butylated Hydroxytoluene | BUTYLATED HYDROXYTOLUENE | 1P9D0Z171K | INJECTION, SOLUTION / INTRAVENOUS | NA | ||
| Butylated Hydroxytoluene | BUTYLATED HYDROXYTOLUENE | 1P9D0Z171K | FILM, SOLUBLE / ORAL | 0.06 mg | ||
| Propylparaben | PROPYLPARABEN | Z8IX2SC1OH | INJECTION, SOLUTION / INTRAVENOUS | 5 mg | ||
| Cetyl Alcohol | CETYL ALCOHOL | 936JST6JCN | SUSPENSION / AURICULAR (OTIC) | 1 %w/v | ||
| Methylparaben | METHYLPARABEN | A2I8C7HI9T | OINTMENT / TOPICAL | 29 mg | ||
| Mineral Oil | MINERAL OIL | T5L8T28FGP | PASTE / TOPICAL | 47.5 %w/w | ||
| Xanthan Gum | XANTHAN GUM | TTV12P4NEE | SOLUTION / ORAL | 84 mg | ||
| Xanthan Gum | XANTHAN GUM | TTV12P4NEE | LOTION / TOPICAL | 0.3 %w/v | ||
| Xanthan Gum | XANTHAN GUM | TTV12P4NEE | TABLET, FILM COATED / ORAL | 0.08 mg | ||
| Butylated Hydroxytoluene | BUTYLATED HYDROXYTOLUENE | 1P9D0Z171K | SWAB / TOPICAL | 0.5 %w/w | ||
| Propylparaben | PROPYLPARABEN | Z8IX2SC1OH | SOLUTION / ORAL | 100 mg | ||
| Glycerin | GLYCERIN | PDC6A3C0OX | SPONGE / TOPICAL | 2 %w/w | ||
| Mineral Oil | MINERAL OIL | T5L8T28FGP | OINTMENT / AURICULAR (OTIC) | NA | ||
| Glycerin | GLYCERIN | PDC6A3C0OX | SUSPENSION/ DROPS / OPHTHALMIC | 2.5 %w/v | ||
| Propylparaben | PROPYLPARABEN | Z8IX2SC1OH | TABLET, EXTENDED RELEASE / ORAL | 0.12 mg | ||
| Glycerin | GLYCERIN | PDC6A3C0OX | INJECTION / INTRAMUSCULAR | 450 mg | ||
| Glycerin | GLYCERIN | PDC6A3C0OX | SUSPENSION / OPHTHALMIC | 58 mg | ||
| Butylated Hydroxytoluene | BUTYLATED HYDROXYTOLUENE | 1P9D0Z171K | CREAM, AUGMENTED / TOPICAL | 0.2 %w/w | ||
| Glycerin | GLYCERIN | PDC6A3C0OX | SOLUTION/ DROPS / OPHTHALMIC | 12 mg | ||
| Glycerin | GLYCERIN | PDC6A3C0OX | CREAM / TOPICAL | 1720 mg | ||
| Propylparaben | PROPYLPARABEN | Z8IX2SC1OH | EMULSION / TOPICAL | 0.06 %w/w | ||
| Propylparaben | PROPYLPARABEN | Z8IX2SC1OH | SOLUTION / RECTAL | 0.02 %w/v | ||
| Cetyl Alcohol | CETYL ALCOHOL | 936JST6JCN | AEROSOL / TOPICAL | 1.16 %w/w | ||
| Methylparaben | METHYLPARABEN | A2I8C7HI9T | PASTE, DENTIFRICE / DENTAL | 0.05 %w/w | ||
| Glycerin | GLYCERIN | PDC6A3C0OX | CREAM, AUGMENTED / TOPICAL | 55 mg | ||
| Petrolatum | PETROLATUM | 4T6H12BN9U | OINTMENT / TOPICAL | 7275 mg | ||
| Propylparaben | PROPYLPARABEN | Z8IX2SC1OH | AEROSOL, FOAM / TOPICAL | 0.04 %w/w | ||
| Potassium Hydroxide | POTASSIUM HYDROXIDE | WZH3C48M4T | CREAM / VAGINAL | 3 mg | ||
| Mineral Oil | MINERAL OIL | T5L8T28FGP | OINTMENT / OPHTHALMIC | 59.5 %w/w | ||
| Glycerin | GLYCERIN | PDC6A3C0OX | TABLET, EXTENDED RELEASE / ORAL | 7 mg | ||
| Methylparaben | METHYLPARABEN | A2I8C7HI9T | TABLET, COATED / ORAL | 0.8 mg | ||
| Sorbitan Monostearate | SORBITAN MONOSTEARATE | NVZ4I0H58X | TABLET / ORAL | 4 mg |
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 |
|---|---|---|---|---|---|---|
| 3e1b23c3-3ef8-4876-ab8b-843f4cfe03cb | eebb8901-cee7-4eac-9c36-ddb64a20742d | 2010-02-01 | Warnings | 3e1b23c3-3ef8-4876-ab8b-843f4cfe03cb eebb8901-cee7-4eac-9c36-ddb64a20742d |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.