Quick answers
- What is Ascorbic acid used for?
- The Drug Facts label of Skin Renewing Serum (Guangzhou Danting Bath&Body Care Industry Co. Ltd) lists these uses: Apply evenly to face and neck daily..
- Do I need a prescription for Ascorbic acid?
- No, the products on this page are sold without a prescription. Other products with the same active ingredient need a prescription (often a higher strength or another form): see the prescription page.
- Is a store brand the same as the name brand?
- Products listed together below have the same active ingredient, in the same amount and the same form, as registered with the FDA. Inactive ingredients (such as colors, flavors and fillers) and package sizes can differ. Compare the “Active ingredient” box on both packages, and ask a pharmacist if you are not sure.
- Has Ascorbic acid been recalled?
- No recall linked to these products appears in the FDA enforcement reports we use.
Also sold by prescription (often at a higher strength or in another form): Ascorbic acid — prescription medicine
Drug Facts label
Every over-the-counter medicine must carry a “Drug Facts” box in the same order, set by FDA rules. Below is the label of one product for each common strength and form, quoted word for word. Your own package can differ (for example, children’s products have other directions): always follow the label on your package.
Skin Renewing Serum · Guangzhou Danting Bath&Body Care Industry Co. Ltd
Ascorbic acid 100 mg/mL, cream (topical)
Active ingredient
Ascorbic Acid 10%
Purpose
Moisturizer
Uses
Apply evenly to face and neck daily.
Warnings
If contact with eyes occurs, rinse thoroughly with water. Avoid eye area
Directions
To brighten skin, hydrate, and moisturize
— FDA label of Skin Renewing Serum, Guangzhou Danting Bath&Body Care Industry Co. Ltd, effective August 23, 2025. See the official label on DailyMed →
Super vitamin C serum · FlexiGo Inc
Ascorbic acid 5.5%, liquid (topical)
Active ingredient
OTC-ACTIVE INGREDIENT SECTION
Purpose
OTC-PURPOSE SECTION
Uses
& USAGE SECTION
Warnings
SECTION OTC-DO NOT USE SECTION OTC-WHEN USING OTC-STOP USE SECTION OTC-KEEP OUT OF REACH OF CHILDREN
Directions
DOSAGE & ADMINISTRATION SECTION
Inactive ingredients
SECTION
— FDA label of Super vitamin C serum, FlexiGo Inc, effective October 22, 2025. See the official label on DailyMed →
This page is not medical advice. Read the label on your package, and ask a pharmacist or doctor if you are not sure a medicine is right for you, for your child, or with your other medicines.
Same medicine, other brands
Each group lists the products that have exactly the same active ingredient, in the same amount and form, as registered with the FDA (NDC Directory). A store brand in the same group has the same medicine as the name brand; inactive ingredients, flavors and package sizes can differ. Each product links to its own official label.
Ascorbic acid 100 mg/mL · cream (topical) · 1 product
Drug Facts for this strength and form ↑
| Brand or product name | Company on the label | Label |
|---|---|---|
| Skin Renewing Serum | Guangzhou Danting Bath&Body Care Industry Co. Ltd | DailyMed |
Ascorbic acid 5.5% · liquid (topical) · 1 product
Drug Facts for this strength and form ↑
| Brand or product name | Company on the label | Label |
|---|---|---|
| Super vitamin C serum | FlexiGo Inc | DailyMed |
Companies that sell this medicine
The company named on the package (maker or distributor), as listed in the FDA NDC Directory, with its number of over-the-counter products of this medicine.
- Guangzhou Danting Bath&Body Care Industry Co. Ltd1 product
- FlexiGo Inc1 product
Recalls
No recall linked to these products (by their NDC code or label) appears in the FDA enforcement reports.
Sources
- Drug labeling (SPL, openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026
- FDA rule for the Drug Facts label (21 CFR 201.66)
Only medicines marketed under FDA rules for nonprescription drugs (an FDA monograph or an FDA approval) are listed. Homeopathic products are not listed: the FDA does not evaluate them for safety or effectiveness.